A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3692391



Internal ID18990672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4417807..4432110hg38UCSC Ensembl
Innerchr9:4417807..4432110hg19UCSC Ensembl
Innerchr9:4407807..4422110hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3814304
hg1914304
hg1814304
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034722
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)nssv3692391
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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