A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3508930



Internal ID18807211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97099985..97176950hg38UCSC Ensembl
Innerchr11:96970985..97047950hg19UCSC Ensembl
Innerchr11:96476195..96553160hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3876966
hg1976966
hg1876966
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050484
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3508930
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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