A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464872



Internal ID22522760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:21339484..21343120hg38UCSC Ensembl
chrX:21357602..21361238hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg383637
hg193637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876689
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17464872
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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