A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736413



Internal ID160079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30624752..30625833hg38UCSC Ensembl
chrX:30642869..30643950hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg381082
hg191082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432871
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736413
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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