A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3579499



Internal ID18877780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:91489004..91661264hg38UCSC Ensembl
Innerchr2:91686694..91849290hg19UCSC Ensembl
Innerchr2:91050421..91213017hg18UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg38172261
hg19162597
hg18162597
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005830
Supporting Variants
Samples
Known GenesLOC654342
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3579499
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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