A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17648411



Internal ID21840458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155803823..155983788hg38UCSC Ensembl
chrX:155033486..155213453hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38179966
hg19179968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6101283
Supporting Variants
Samples
Known GenesVAMP7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17648411
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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