A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv711876



Internal ID16005832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25740970..25795606hg38UCSC Ensembl
Innerchr1:26067461..26122097hg19UCSC Ensembl
Innerchr1:25940048..25994684hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3854637
hg1954637
hg1854637
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545882
Supporting Variants
Samples
Known GenesMAN1C1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv711876
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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