A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515965



Internal ID15096572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:17273458..17309480hg38UCSC Ensembl
Innerchr19:17384267..17420289hg19UCSC Ensembl
Innerchr19:17245267..17281289hg18UCSC Ensembl
Innerchr19:17245267..17281289hg17UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3836023
hg1936023
hg1836023
hg1736023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703068, nssv662122, nssv673562, nssv675433, nssv702549, nssv662342, nssv658228, nssv672661, nssv659424, nssv679225, nssv676858, nssv677944, nssv688468, nssv665495
Samples
Known GenesABHD8, ANKLE1, BABAM1, MRPL34
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515965
Frequency
Sample Size2026
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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