A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102685



Internal ID22011918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:14205554..14205832hg38UCSC Ensembl
chrX:14223676..14223954hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644696
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102685
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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