A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18132132



Internal ID20699172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:71931669..71931913hg38UCSC Ensembl
chr5:71227496..71227740hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414957
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18132132
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00165


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