A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737510



Internal ID161176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123967300..123974200hg38UCSC Ensembl
chrX:123101150..123108050hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg386901
hg196901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433241
Supporting Variants
Samples
Known GenesSTAG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737510
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00251362


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