A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515663



Internal ID15443274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149235238..149255678hg38UCSC Ensembl
Innerchr3:148953025..148973465hg19UCSC Ensembl
Innerchr3:150435715..150456155hg18UCSC Ensembl
Innerchr3:150435723..150456163hg17UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3820441
hg1920441
hg1820441
hg1720441
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv301n21
Supporting Variantsnssv673381, nssv670804, nssv664087, nssv665067, nssv669647, nssv667547, nssv693293, nssv688813, nssv668294, nssv681287, nssv659129, nssv671781, nssv679922, nssv658678, nssv686644, nssv671718, nssv676201, nssv667798, nssv680655, nssv670026, nssv654936, nssv657301, nssv655667, nssv676641, nssv685338, nssv691161, nssv682352, nssv660518, nssv680631, nssv682204, nssv684868, nssv688009, nssv655971, nssv659089, nssv654809, nssv678775, nssv658109, nssv675580, nssv679340, nssv674279, nssv662384, nssv676221, nssv691794, nssv688155, nssv683543, nssv691774, nssv692517, nssv651988, nssv690048, nssv681927, nssv660079, nssv669850, nssv655886, nssv659918, nssv675546, nssv686314, nssv662628, nssv676521, nssv666697, nssv684834, nssv672739, nssv655039, nssv677477, nssv673754, nssv668990, nssv671986, nssv656165, nssv663626, nssv677454, nssv664259, nssv656013, nssv658934, nssv668734, nssv685539, nssv693722, nssv652693, nssv656236, nssv680193, nssv693548, nssv662838, nssv651953, nssv682756, nssv670402
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515663
Frequency
Sample Size2026
Observed Gain0
Observed Loss83
Observed Complex0
Frequencyn/a


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