A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839475



Internal ID16133431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30361487..30457607hg38UCSC Ensembl
Innerchr15:30653690..30749810hg19UCSC Ensembl
Innerchr15:28440982..28537102hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3896121
hg1996121
hg1896121
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568746
Supporting Variants
Samples
Known GenesCHRFAM7A, LOC101059918
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv839475
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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