A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569648



Internal ID16357057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:61947498..62047927hg38UCSC Ensembl
Innerchr15:62239697..62340126hg19UCSC Ensembl
Innerchr15:60026989..60127418hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38100430
hg19100430
hg18100430
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843669
Samples
Known GenesVPS13C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569648
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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