A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138524



Internal ID337708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119949200..119966100hg38UCSC Ensembl
chrX:119083163..119100063hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3816901
hg1916901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737359
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138524
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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