A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138923



Internal ID338107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:65173600..65201500hg38UCSC Ensembl
chrX:64393480..64421380hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg3827901
hg1927901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740390
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138923
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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