A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737462



Internal ID161128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123013381..123020000hg38UCSC Ensembl
chrX:122147234..122153853hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg386620
hg196620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138428
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737462
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0027208


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