A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616598



Internal ID20989669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169539601..169704000hg38UCSC Ensembl
chr6:169939697..170104096hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38164400
hg19164400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216140
Samples
Known GenesC6orf120, PHF10, WDR27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616598
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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