A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604292



Internal ID20977363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169644101..169762500hg38UCSC Ensembl
chr6:170044197..170162596hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38118400
hg19118400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216143
Samples
Known GenesC6orf120, ERMARD, PHF10, TCTE3, WDR27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604292
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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