A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350635



Internal ID21008188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:189285683..189286150hg38UCSC Ensembl
chr2:190150409..190150876hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg38468
hg19468
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083512
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350635
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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