A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364210



Internal ID21021763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56745839..56756613hg38UCSC Ensembl
chr3:56779867..56790641hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3810775
hg1910775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102856
Samples
Known GenesARHGEF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364210
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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