A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1028855



Internal ID15535355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:31629019..31649431hg38UCSC Ensembl
Innerchr5:31629126..31649538hg19UCSC Ensembl
Innerchr5:31664883..31685295hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3820413
hg1920413
hg1820413
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597764
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)nssv1028855
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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