A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3758117



Internal ID19056398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7735283..7772912hg38UCSC Ensembl
Innerchr9:7735283..7772912hg19UCSC Ensembl
Innerchr9:7725283..7762912hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3837630
hg1937630
hg1837630
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025200
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)nssv3758117
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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