A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17641633



Internal ID21833680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48625765..48629200hg38UCSC Ensembl
chrX:48484153..48487588hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg383436
hg193436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6101341
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17641633
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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