A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2810939



Internal ID21256277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:31203676..31203676hg38UCSC Ensembl
chr4:31205298..31205298hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13685755
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2810939
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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