A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17642872



Internal ID21834919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:74744891..74744958hg38UCSC Ensembl
chrX:73964726..73964793hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6111807
Supporting Variants
Samples
Known GenesKIAA2022
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17642872
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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