A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615445



Internal ID20988516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138883585..138902621hg38UCSC Ensembl
chr6:139204722..139223758hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3819037
hg1919037
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216866
Samples
Known GenesECT2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615445
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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