A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739099



Internal ID162765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:7067596..7196706hg38UCSC Ensembl
chrX:6985637..7114747hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38129111
hg19129111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426709
Supporting Variants
Samples
Known GenesHDHD1, MIR4767
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739099
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000208117


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