A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3465712



Internal ID18714671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25247968..25292537hg38UCSC Ensembl
Innerchr1:25574459..25619028hg19UCSC Ensembl
Innerchr1:25447046..25491615hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3844570
hg1944570
hg1844570
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007623
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)nssv3465712
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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