A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431741



Internal ID22489611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:122435458..122435458hg38UCSC Ensembl
chrX:121569311..121569311hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5953494
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431741
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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