A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6137878



Internal ID337059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:16394000..16402300hg38UCSC Ensembl
chrX:16412123..16420423hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg388301
hg198301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739428
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6137878
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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