A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604298



Internal ID20977369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160930777..161147177hg38UCSC Ensembl
chr6:161351809..161568209hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38216401
hg19216401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216736
Samples
Known GenesAGPAT4, MAP3K4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604298
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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