A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3693002



Internal ID18991283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42729314..42856259hg38UCSC Ensembl
Innerchr9:44114860..44241805hg19UCSC Ensembl
Innerchr9:44054856..44181801hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38126946
hg19126946
hg18126946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020826
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)nssv3693002
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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