A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517399



Internal ID15444692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:51974681..52013267hg38UCSC Ensembl
Innerchr15:52266878..52305464hg19UCSC Ensembl
Innerchr15:50054170..50092756hg18UCSC Ensembl
Innerchr15:50054170..50092756hg17UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3838587
hg1938587
hg1838587
hg1738587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv681736, nssv662680, nssv676006, nssv676280, nssv667497, nssv663778, nssv654804, nssv678772, nssv698150, nssv689841, nssv678390, nssv654690, nssv657809, nssv692512, nssv702403, nssv662423, nssv656162, nssv673159, nssv688482, nssv683432, nssv682435, nssv690284, nssv658594, nssv687192, nssv660055, nssv656472, nssv693405, nssv674586, nssv678456, nssv678240, nssv658637, nssv657558, nssv651906, nssv666613, nssv652168
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517399
Frequency
Sample Size2026
Observed Gain0
Observed Loss35
Observed Complex0
Frequencyn/a


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