A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615751



Internal ID20988822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112379344..112452926hg38UCSC Ensembl
chr6:112700546..112774128hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3873583
hg1973583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135463
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615751
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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