A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17641071



Internal ID21833118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:70208850..70234170hg38UCSC Ensembl
chrX:69428700..69454020hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3825321
hg1925321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6101064
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17641071
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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