A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3580035



Internal ID18878316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:97360488..97652647hg38UCSC Ensembl
Innerchr2:98013814..98269110hg19UCSC Ensembl
Innerchr2:97379953..97635542hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38292160
hg19255297
hg18255590
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010905
Supporting Variants
Samples
Known GenesANKRD36B, COX5B, LOC100506076, LOC100506123
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3580035
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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