A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390497



Internal ID21048050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70293358..70421489hg38UCSC Ensembl
chr4:71159075..71287206hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38128132
hg19128132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119098
Samples
Known GenesCABS1, PROL1, SMR3A, SMR3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390497
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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