A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5420505



Internal ID199607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:5034506..5038870hg38UCSC Ensembl
chrX:4952547..4956911hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg384365
hg194365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736180
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5420505
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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