A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352996



Internal ID21010549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26566992..26582698hg38UCSC Ensembl
chr2:26789860..26805566hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3815707
hg1915707
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209128
Samples
Known GenesC2orf70, CIB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352996
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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