A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5416585



Internal ID195805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:38496989..38497635hg38UCSC Ensembl
chrX:38356242..38356888hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38647
hg19647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736445
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5416585
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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