A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17639155



Internal ID21831202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:134613496..134613496hg38UCSC Ensembl
chrX:133747526..133747526hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg382223
hg192223
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6056489
Supporting Variants
Samples
Known GenesPLAC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17639155
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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