A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102377



Internal ID22011611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:100611217..100611289hg38UCSC Ensembl
chrX:99866214..99866286hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648264
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102377
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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