A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17639010



Internal ID21831057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123864778..123864848hg38UCSC Ensembl
chrX:122998628..122998698hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6112337
Supporting Variants
Samples
Known GenesXIAP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17639010
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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