A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2789597



Internal ID21234935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17849123..17849123hg38UCSC Ensembl
chr10:18138052..18138052hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg386243
hg196243
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13689478
Samples
Known GenesMRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2789597
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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