A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3484822



Internal ID19072463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:218683402..218825530hg38UCSC Ensembl
Innerchr1:218856744..218998872hg19UCSC Ensembl
Innerchr1:216923367..217065495hg18UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38142129
hg19142129
hg18142129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002772
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)nssv3484822
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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