A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568737



Internal ID16009460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30276146..30537608hg38UCSC Ensembl
Innerchr15:30568349..30829811hg19UCSC Ensembl
Innerchr15:28355641..28617103hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38261463
hg19261463
hg18261463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4419n54
Supporting Variantsnssv839464
Samples
Known GenesCHRFAM7A, LOC101059918
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568737
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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