A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739100



Internal ID162766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:7083169..7083274hg38UCSC Ensembl
chrX:7001210..7001315hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420583
Supporting Variants
Samples
Known GenesHDHD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739100
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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