A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4006664



Internal ID22068295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:77155590..77162488hg38UCSC Ensembl
Outerchr9:77155482..77171212hg38UCSC Ensembl
Innerchr9:79770506..79777404hg19UCSC Ensembl
Outerchr9:79770398..79786128hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg3815731
hg1915731
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154516
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4006664
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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