A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740714



Internal ID164380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:73112271..73123000hg38UCSC Ensembl
chrX:72332110..72342839hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3810730
hg1910730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5414082
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740714
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00668757


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