A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372597



Internal ID21030150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3037645..3039426hg38UCSC Ensembl
chr4:3039372..3041153hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381782
hg191782
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114150
Samples
Known GenesGRK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372597
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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