A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3759781



Internal ID19058062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:84052078..84086997hg38UCSC Ensembl
Innerchr9:86666993..86701912hg19UCSC Ensembl
Innerchr9:85856813..85891732hg18UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3834920
hg1934920
hg1834920
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045322
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)nssv3759781
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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