A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13696788



Internal ID21218645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:16183259..16183259hg38UCSC Ensembl
chrX:16201382..16201382hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38608
hg19608
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2820294
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13696788
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.25


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