A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697561



Internal ID18995842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:93885658..93927045hg38UCSC Ensembl
Innerchr9:96647940..96689327hg19UCSC Ensembl
Innerchr9:95687761..95729148hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3841388
hg1941388
hg1841388
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046904
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)nssv3697561
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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