A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353348



Internal ID21010901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:70735922..70737315hg38UCSC Ensembl
chr2:70963054..70964447hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg381394
hg191394
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207007
Samples
Known GenesADD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353348
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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