A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741176



Internal ID164842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:85254313..85254646hg38UCSC Ensembl
chrX:84509319..84509652hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415743
Supporting Variants
Samples
Known GenesZNF711
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741176
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.208463


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