A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353134



Internal ID21010687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:60976565..61000115hg38UCSC Ensembl
chr2:61203700..61227250hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3823551
hg1923551
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206364
Samples
Known GenesPUS10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353134
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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