A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690634



Internal ID18988915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:16022188..16064160hg38UCSC Ensembl
Innerchr9:16022186..16064158hg19UCSC Ensembl
Innerchr9:16012186..16054158hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3841973
hg1941973
hg1841973
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025555
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)nssv3690634
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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