A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736799



Internal ID160465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47506781..47522313hg38UCSC Ensembl
chrX:47366180..47381712hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3815533
hg1915533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5429174
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736799
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000832466


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