A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1057782



Internal ID15564282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33656956..33682966hg38UCSC Ensembl
Innerchr6:33624733..33650743hg19UCSC Ensembl
Innerchr6:33732711..33758721hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3826011
hg1926011
hg1826011
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602838
Supporting Variants
Samples
Known GenesITPR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1057782
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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