A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519561



Internal ID15100168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6745094..6774058hg38UCSC Ensembl
Innerchr19:6745105..6774069hg19UCSC Ensembl
Innerchr19:6696105..6725069hg18UCSC Ensembl
Innerchr19:6696105..6725069hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3828965
hg1928965
hg1828965
hg1728965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv690240, nssv692917, nssv691061, nssv688524, nssv672591, nssv656886, nssv691521
Samples
Known GenesSH2D3A, TRIP10, VAV1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519561
Frequency
Sample Size2026
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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