A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041737



Internal ID95531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6950500..6975000hg38UCSC Ensembl
chr11:6971731..6996231hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3824501
hg1924501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5505774
Supporting Variants
Samples
Known GenesZNF215
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041737
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000313


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