A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17433699



Internal ID22491569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:112992410..112992410hg38UCSC Ensembl
chrX:112235638..112235638hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5949590
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17433699
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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