A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604004



Internal ID20977075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:127502604..127566543hg38UCSC Ensembl
chr6:127823749..127887688hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg3863940
hg1963940
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215522
Samples
Known GenesSOGA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604004
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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