A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737276



Internal ID160942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:118439363..118439862hg38UCSC Ensembl
chrX:117573326..117573825hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6139024
Supporting Variants
Samples
Known GenesWDR44
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737276
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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