A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17640207



Internal ID21832254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:131395247..131396837hg38UCSC Ensembl
chrX:130529221..130530811hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg381591
hg191591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6111080
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17640207
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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