A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359237



Internal ID21016790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:23837212..23837817hg38UCSC Ensembl
chr4:23838835..23839440hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38606
hg19606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113311
Samples
Known GenesPPARGC1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359237
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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