A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18160143



Internal ID20727183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:69425805..69426352hg38UCSC Ensembl
chr7:68890791..68891338hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38548
hg19548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6618610
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18160143
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00045


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