A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340872



Internal ID20998425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231314281..231328198hg38UCSC Ensembl
chr2:232178994..232192910hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3813918
hg1913917
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086569
Samples
Known GenesARMC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340872
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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