A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2793165



Internal ID21238503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:92347883..92347883hg38UCSC Ensembl
chr13:93000136..93000136hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13680514
Samples
Known GenesGPC5
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2793165
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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