A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001763



Internal ID19090980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:8517172..8551029hg38UCSC Ensembl
Innerchr2:8657302..8691159hg19UCSC Ensembl
Innerchr2:8574753..8608610hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3833858
hg1933858
hg1833858
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3713n100
Supporting Variantsnssv3576944, nssv3576943
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)nsv1001763
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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