A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13708946



Internal ID21230730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49181566..49181566hg38UCSC Ensembl
chrX:49037916..49037916hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2820388
Supporting Variants
Samples
Known GenesPRICKLE3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13708946
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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