A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1012981



Internal ID16306937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:170150280..170155411hg38UCSC Ensembl
Innerchr4:171071431..171076562hg19UCSC Ensembl
Innerchr4:171308006..171313137hg18UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg385132
hg195132
hg185132
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596139
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)nssv1012981
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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