A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3700864



Internal ID18652459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25256126..25319681hg38UCSC Ensembl
Innerchr1:25582617..25646172hg19UCSC Ensembl
Innerchr1:25455204..25518759hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3863556
hg1963556
hg1863556
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006870
Supporting Variants
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)nssv3700864
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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