A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3757327



Internal ID19055608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:98533265..98594865hg38UCSC Ensembl
Innerchr8:99545493..99607093hg19UCSC Ensembl
Innerchr8:99614669..99676269hg18UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3861601
hg1961601
hg1861601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030498
Supporting Variants
Samples
Known GenesSTK3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3757327
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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