A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3692149



Internal ID18990430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61627300hg38UCSC Ensembl
Innerchr9:44727847..44835138hg19UCSC Ensembl
Innerchr9:44667843..44775134hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38107292
hg19107292
hg18107292
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031249
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)nssv3692149
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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