A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139070



Internal ID338254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:143278161..143431792hg38UCSC Ensembl
chrX:142365938..142519586hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38153632
hg19153649
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737675
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139070
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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