A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18146998



Internal ID20714038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107903150..107912065hg38UCSC Ensembl
chr7:107543595..107552510hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg388916
hg198916
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602241
Supporting Variants
Samples
Known GenesDLD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18146998
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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