A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350152



Internal ID21007705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:186836101..186860300hg38UCSC Ensembl
chr2:187700828..187725027hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3824200
hg1924200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205385
Samples
Known GenesZSWIM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350152
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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