A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366874



Internal ID21024427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7516030..7530276hg38UCSC Ensembl
chr4:7517757..7532003hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3814247
hg1914247
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212367
Samples
Known GenesSORCS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366874
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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