A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387975



Internal ID21045528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47604373..47656602hg38UCSC Ensembl
chr4:47606390..47658619hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3852230
hg1952230
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211878
Samples
Known GenesCORIN, MIR8053
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387975
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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