A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17646421



Internal ID21838468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46847799..46847799hg38UCSC Ensembl
chrX:46707234..46707234hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6051145
Supporting Variants
Samples
Known GenesRP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17646421
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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