A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1045487



Internal ID15898673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:172882576..172918983hg38UCSC Ensembl
Innerchr5:172309579..172345986hg19UCSC Ensembl
Innerchr5:172242185..172278592hg18UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3836408
hg1936408
hg1836408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv600295
Supporting Variants
Samples
Known GenesERGIC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1045487
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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