A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738001



Internal ID161667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152005000..152015606hg38UCSC Ensembl
chrX:151173472..151184078hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3810607
hg1910607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138887
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738001
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00272251


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