A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697579



Internal ID18995860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102105789..102280443hg38UCSC Ensembl
Innerchr9:104868071..105042725hg19UCSC Ensembl
Innerchr9:103907892..104082546hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38174655
hg19174655
hg18174655
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052675
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)nssv3697579
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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