A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1021335



Internal ID16315291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:668222..696435hg38UCSC Ensembl
Innerchr5:668337..696550hg19UCSC Ensembl
Innerchr5:721337..749550hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3828214
hg1928214
hg1828214
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596713
Supporting Variants
Samples
Known GenesTPPP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1021335
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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