A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138561



Internal ID337745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46455837..46478000hg38UCSC Ensembl
chrX:46315272..46337435hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3822164
hg1922164
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736751
Samples
Known GenesKRBOX4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138561
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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