A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387778



Internal ID21045331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158997265..158997687hg38UCSC Ensembl
chr4:159918417..159918839hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212763
Samples
Known GenesC4orf45
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387778
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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