A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146104



Internal ID345309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81861133..81899133hg38UCSC Ensembl
chr17:79819009..79857009hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3838001
hg1938001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17715618
Samples
Known GenesALYREF, ANAPC11, ARHGDIA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146104
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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