A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739542



Internal ID163208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:19617196..19617503hg38UCSC Ensembl
chrX:19635314..19635621hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424717
Supporting Variants
Samples
Known GenesSH3KBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739542
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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