A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645649



Internal ID21837696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:81229463..81230980hg38UCSC Ensembl
chrX:80484962..80486479hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg381518
hg191518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106167
Supporting Variants
Samples
Known GenesSH3BGRL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645649
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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