A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608084



Internal ID20981155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138735311..138738052hg38UCSC Ensembl
chr6:139056448..139059189hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg382742
hg192742
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216861
Samples
Known GenesLOC100507462
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608084
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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