A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729795



Internal ID19028076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88846299..89245848hg38UCSC Ensembl
Innerchr2:89145812..89545331hg19UCSC Ensembl
Innerchr2:88926927..89326446hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38399550
hg19399520
hg18399520
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012724
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)nssv3729795
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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