A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605491



Internal ID20978562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138155901..138168000hg38UCSC Ensembl
chr6:138477038..138489137hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3812100
hg1912100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216856
Samples
Known GenesKIAA1244
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605491
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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