A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138261



Internal ID337445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:106086542..106111000hg38UCSC Ensembl
chrX:105330533..105354992hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3824459
hg1924460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741813
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138261
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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