A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601054



Internal ID20974125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169352225..169657324hg38UCSC Ensembl
chr6:169752320..170057420hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38305100
hg19305101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216138
Samples
Known GenesWDR27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601054
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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