A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412536



Internal ID21070089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37750867..37753420hg38UCSC Ensembl
chr6:37718643..37721196hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg382554
hg192554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141820
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412536
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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