A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv711710



Internal ID15658980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25271785..25320442hg38UCSC Ensembl
Innerchr1:25598276..25646933hg19UCSC Ensembl
Innerchr1:25470863..25519520hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3848658
hg1948658
hg1848658
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545836
Supporting Variants
Samples
Known GenesRHD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv711710
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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