A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645033



Internal ID21837080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102694426..102694426hg38UCSC Ensembl
chrX:101949354..101949354hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg382284
hg192284
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6059642
Supporting Variants
Samples
Known GenesARMCX5-GPRASP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645033
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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