A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439041



Internal ID22496911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:14507689..14507689hg38UCSC Ensembl
chrX:14525811..14525811hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5961055
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439041
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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