A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613976



Internal ID20987047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138794801..138799900hg38UCSC Ensembl
chr6:139115938..139121037hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216863
Samples
Known GenesECT2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613976
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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