A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003163



Internal ID18745694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25247968..25320186hg38UCSC Ensembl
Innerchr1:25574459..25646677hg19UCSC Ensembl
Innerchr1:25447046..25519264hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3872219
hg1972219
hg1872219
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv134n100
Supporting Variantsnssv3468542
Samples
Known GenesRHD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003163
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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