A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1035779



Internal ID15888965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:85815317..85902372hg38UCSC Ensembl
Innerchr5:85111135..85198190hg19UCSC Ensembl
Innerchr5:85146891..85233946hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3887056
hg1987056
hg1887056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598831
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)nssv1035779
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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