A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138862



Internal ID338046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2988442..3020275hg38UCSC Ensembl
chrX:2906483..2938316hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3831834
hg1931834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736088
Samples
Known GenesARSH
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138862
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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