A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695221



Internal ID18646816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:121750763..121831165hg38UCSC Ensembl
Innerchr9:124513042..124593444hg19UCSC Ensembl
Innerchr9:123552863..123633265hg18UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3880403
hg1980403
hg1880403
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053662
Supporting Variants
Samples
Known GenesDAB2IP, MIR548AA1, MIR548D1, TTLL11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3695221
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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