A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645399



Internal ID21837446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:38507518..38515276hg38UCSC Ensembl
chrX:38366771..38374529hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg387759
hg197759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103795
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645399
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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