A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17639956



Internal ID21832003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3072439..3072566hg38UCSC Ensembl
chrX:2990480..2990607hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6102716
Supporting Variants
Samples
Known GenesARSF
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17639956
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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