A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108527



Internal ID22017760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102676282..102676391hg38UCSC Ensembl
chrX:101931210..101931319hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643853
Samples
Known GenesARMCX5-GPRASP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108527
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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