A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361108



Internal ID21018661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:879189..879598hg38UCSC Ensembl
chr4:872977..873386hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18121802
Samples
Known GenesGAK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361108
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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