A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376937



Internal ID21034490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:51975689..52000118hg38UCSC Ensembl
chr4:52841855..52866284hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3824430
hg1924430
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211894
Samples
Known GenesLRRC66
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376937
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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