A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464070



Internal ID22521956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:82688725..82690900hg38UCSC Ensembl
chrX:81944174..81946349hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg382176
hg192176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872274
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464070
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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