A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138428



Internal ID337612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123013381..123020000hg38UCSC Ensembl
chrX:122147234..122153853hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg386620
hg196620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737462
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138428
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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