A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609112



Internal ID20982183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106703339..106704203hg38UCSC Ensembl
chr6:107151214..107152078hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38865
hg19865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136885
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609112
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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