A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609277



Internal ID20982348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139982390..139982977hg38UCSC Ensembl
chr6:140303527..140304114hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138518
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609277
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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