A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13697150



Internal ID21218999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:105054591..105054698hg38UCSC Ensembl
chr2:105671049..105671156hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2804670
Supporting Variants
Samples
Known GenesMRPS9
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13697150
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.296875


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