A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339234



Internal ID20996787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:112715737..112719809hg38UCSC Ensembl
chr2:113473314..113477386hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg384073
hg194073
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206489
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339234
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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