A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339196



Internal ID20996749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:236038644..236136999hg38UCSC Ensembl
chr2:236947288..237045643hg19UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg3898356
hg1998356
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208350
Samples
Known GenesAGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339196
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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