A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18159932



Internal ID20726972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:9172359..9324846hg38UCSC Ensembl
chr7:9211989..9364476hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38152488
hg19152488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619520
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18159932
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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