A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366901



Internal ID21024454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2204041..2205807hg38UCSC Ensembl
chr4:2205768..2207534hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381767
hg191767
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116128
Samples
Known GenesPOLN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366901
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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