A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367949



Internal ID21025502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2518676..2523441hg38UCSC Ensembl
chr4:2520403..2525168hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg384766
hg194766
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211794
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367949
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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