A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612596



Internal ID20985667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:140454654..140543103hg38UCSC Ensembl
chr6:140775791..140864240hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3888450
hg1988450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6428n223
Supporting Variantsnssv18138570
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612596
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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