A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5415046



Internal ID194309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:7290865..7293341hg38UCSC Ensembl
chrX:7208906..7211382hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg382477
hg192477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739107
Samples
Known GenesSTS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5415046
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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