A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2790146



Internal ID21235484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70918574..70918666hg38UCSC Ensembl
chr10:72678331..72678423hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13687254
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2790146
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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