A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387991



Internal ID21045544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40757124..40758787hg38UCSC Ensembl
chr4:40759141..40760804hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381664
hg191664
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213623
Samples
Known GenesNSUN7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387991
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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