A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013649



Internal ID19102868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:6103342..6805887hg38UCSC Ensembl
Innerchr2:6243474..6946018hg19UCSC Ensembl
Innerchr2:6160925..6863469hg18UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg38702546
hg19702545
hg18702545
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3711n100
Supporting Variantsnssv3576931
Samples
Known GenesLINC00487, MIR7515
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013649
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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