A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101693



Internal ID22010926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119286378..119340544hg38UCSC Ensembl
chrX:118420341..118474507hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3854167
hg1954167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646092
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101693
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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