A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13694506



Internal ID21216358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124471567..124471567hg38UCSC Ensembl
chr10:126160136..126160136hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2788362
Supporting Variants
Samples
Known GenesLHPP
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13694506
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.111111


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