A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1050876



Internal ID15557376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:19837856..19839050hg38UCSC Ensembl
Innerchr6:19838087..19839281hg19UCSC Ensembl
Innerchr6:19946066..19947260hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381195
hg191195
hg181195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601089
Supporting Variants
Samples
Known GenesID4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1050876
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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