A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335804



Internal ID20993357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231361541..231374425hg38UCSC Ensembl
chr2:232226252..232239136hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3812885
hg1912885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086574
Samples
Known GenesARMC9, MIR4777
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335804
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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