A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5433538



Internal ID212250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71931394..71931637hg38UCSC Ensembl
chrX:71151244..71151487hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740679
Samples
Known GenesNHSL2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5433538
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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