A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379247



Internal ID21036800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:146169601..146178400hg38UCSC Ensembl
chr4:147090753..147099552hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg388800
hg198800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212028
Samples
Known GenesLSM6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379247
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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