A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697559



Internal ID18995840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:93882594..93920932hg38UCSC Ensembl
Innerchr9:96644876..96683214hg19UCSC Ensembl
Innerchr9:95684697..95723035hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3838339
hg1938339
hg1838339
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053137
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)nssv3697559
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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