A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695552



Internal ID18993833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61680277hg38UCSC Ensembl
Innerchr9:44727847..44888115hg19UCSC Ensembl
Innerchr9:44667843..44828111hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38160269
hg19160269
hg18160269
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023804
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)nssv3695552
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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