A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739292



Internal ID162958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:12744294..12744393hg38UCSC Ensembl
chrX:12762413..12762512hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425999
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739292
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.135696


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