A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740073



Internal ID163739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:36650006..36719611hg38UCSC Ensembl
chrX:36668079..36737684hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3869606
hg1969606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420206
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740073
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00270552


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