A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737996



Internal ID161662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151765606..151770700hg38UCSC Ensembl
chrX:150934078..150939172hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg385095
hg195095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5428829
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737996
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00313873


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