A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17448339



Internal ID22506209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103103389..103105571hg38UCSC Ensembl
chrX:102358317..102360499hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg382183
hg192183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5884769
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17448339
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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