A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437274



Internal ID22495144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103437058..103437058hg38UCSC Ensembl
chrX:102691986..102691986hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5963575
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437274
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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