A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17466766



Internal ID22524657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:93931812..93932987hg38UCSC Ensembl
chrX:93186811..93187986hg19UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg381176
hg191176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5883105
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17466766
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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