A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3472569



Internal ID18718355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25256126..25320483hg38UCSC Ensembl
Innerchr1:25582617..25646974hg19UCSC Ensembl
Innerchr1:25455204..25519561hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3864358
hg1964358
hg1864358
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006754
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)nssv3472569
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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