A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337010



Internal ID20994563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231474024..231641642hg38UCSC Ensembl
chr2:232338735..232506353hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38167619
hg19167619
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206204
Samples
Known GenesC2orf57, LINC00471, NMUR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337010
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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