A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695220



Internal ID18646815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:121522791..121618643hg38UCSC Ensembl
Innerchr9:124285070..124380922hg19UCSC Ensembl
Innerchr9:123324891..123420743hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3895853
hg1995853
hg1895853
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037310
Supporting Variants
Samples
Known GenesDAB2IP, MIR548AA1, MIR548D1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3695220
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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