A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv718358



Internal ID16012314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:80816549..80878873hg38UCSC Ensembl
Innerchr1:81282234..81344558hg19UCSC Ensembl
Innerchr1:81054822..81117146hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3862325
hg1962325
hg1862325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546673
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv718358
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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