A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352691



Internal ID21010244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61063157..61173325hg38UCSC Ensembl
chr2:61290292..61400460hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38110169
hg19110169
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206366
Samples
Known GenesC2orf74, KIAA1841, LOC339803
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352691
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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