A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638639



Internal ID21830686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:7734202..7753411hg38UCSC Ensembl
chrX:7702243..7721452hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3819210
hg1919210
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6100485
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638639
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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