A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18156901



Internal ID20723941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20582638..20589594hg38UCSC Ensembl
chr7:20622261..20629217hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg386957
hg196957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602047
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18156901
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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