A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352989



Internal ID21010542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:190059001..190059900hg38UCSC Ensembl
chr2:190923727..190924626hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083250
Samples
Known GenesMSTN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352989
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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