A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468918



Internal ID22526808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3483921..3484009hg38UCSC Ensembl
chrX:3401962..3402050hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875516
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468918
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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