A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17648449



Internal ID21840496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:73109735..73123384hg38UCSC Ensembl
chrX:72329574..72343223hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3813650
hg1913650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6105534
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17648449
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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