A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138569



Internal ID337753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:136083381..136089700hg38UCSC Ensembl
chrX:135165540..135171859hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg386320
hg196320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742526
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138569
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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