A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545861



Internal ID15986584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25303147..25320442hg38UCSC Ensembl
Innerchr1:25629638..25646933hg19UCSC Ensembl
Innerchr1:25502225..25519520hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3817296
hg1917296
hg1817296
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv711801
Samples
Known GenesRHD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545861
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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