A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618120



Internal ID20991191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:140057744..140071235hg38UCSC Ensembl
chr6:140378881..140392372hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3813492
hg1913492
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138529
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618120
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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