A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638215



Internal ID21830262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:26833244..26833244hg38UCSC Ensembl
chrX:26851361..26851361hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg383333
hg193333
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040534
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638215
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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