A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269670



Internal ID20478888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:53578315..53578645hg38UCSC Ensembl
chrX:53605275..53605605hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758420
Supporting Variants
Samples
Known GenesHUWE1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269670
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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