A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17646267



Internal ID21838314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:75552131..75620058hg38UCSC Ensembl
chrX:74771966..74839893hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg3867928
hg1967928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106190
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17646267
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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