A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1021492



Internal ID15968762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1009968..1190946hg38UCSC Ensembl
Innerchr5:1010083..1191061hg19UCSC Ensembl
Innerchr5:1063083..1244061hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38180979
hg19180979
hg18180979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596802
Supporting Variants
Samples
Known GenesMIR4635, NKD2, SLC12A7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1021492
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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