A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690679



Internal ID18988960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19145272..19208993hg38UCSC Ensembl
Innerchr9:19145270..19208991hg19UCSC Ensembl
Innerchr9:19135270..19198991hg18UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3863722
hg1963722
hg1863722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017603
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)nssv3690679
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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