A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5428412



Internal ID207283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:37714996..37720243hg38UCSC Ensembl
chrX:37574249..37579496hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg385248
hg195248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736422
Samples
Known GenesXK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5428412
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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