A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17640742



Internal ID21832789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:72726004..72726004hg38UCSC Ensembl
chrX:71945857..71945857hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg382724
hg192724
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6060235
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17640742
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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