A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147184



Internal ID346366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54853651..54859470hg38UCSC Ensembl
chrX:54880084..54885903hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg385820
hg195820
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740172
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147184
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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