A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347580



Internal ID21005133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231201842..231211537hg38UCSC Ensembl
chr2:232066555..232076250hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg389696
hg199696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086562
Samples
Known GenesARMC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347580
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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