A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515629



Internal ID15096236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:96217861..96222332hg38UCSC Ensembl
Innerchr14:96684198..96688669hg19UCSC Ensembl
Innerchr14:95753951..95758422hg18UCSC Ensembl
Innerchr14:95753951..95758422hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg384472
hg194472
hg184472
hg174472
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv672617, nssv668421, nssv662318, nssv657771, nssv673601, nssv669173, nssv664161, nssv686867, nssv667265, nssv678093, nssv674250, nssv659713
Samples
Known GenesBDKRB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515629
Frequency
Sample Size2026
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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