A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645467



Internal ID21837514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48584220..48584279hg38UCSC Ensembl
chrX:48442608..48442667hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6107665
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645467
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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