A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999939



Internal ID19159475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:91426526..91626091hg38UCSC Ensembl
Innerchr2:91618895..91814117hg19UCSC Ensembl
Innerchr2:90982622..91177844hg18UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg38199566
hg19195223
hg18195223
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3990n100
Supporting Variantsnssv3579420
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)nsv999939
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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