A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138845



Internal ID338029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:26955488..27020500hg38UCSC Ensembl
chrX:26973605..27038617hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3865013
hg1965013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736267
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138845
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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