A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138386



Internal ID337570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:80712106..80713781hg38UCSC Ensembl
chrX:79967605..79969280hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg381676
hg191676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741002
Samples
Known GenesBRWD3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138386
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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