A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18153099



Internal ID20720139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35064020..35073883hg38UCSC Ensembl
chr7:35103632..35113495hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg389864
hg199864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6603677
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18153099
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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