A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13679954



Internal ID21201815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101855064..101855064hg38UCSC Ensembl
chr10:103614821..103614821hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg381514
hg191514
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2788436
Supporting Variants
Samples
Known GenesC10orf76
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13679954
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.9


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