A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387403



Internal ID21044956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55296465..55300451hg38UCSC Ensembl
chr4:56162632..56166618hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg383987
hg193987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18118356
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387403
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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