A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18160909



Internal ID20727949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81528774..81529286hg38UCSC Ensembl
chr7:81158090..81158602hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606692
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18160909
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00039


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