A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496743



Internal ID20869946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37070077..37120233hg38UCSC Ensembl
chr17:35427369..35477155hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3850157
hg1949787
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179092
Samples
Known GenesACACA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496743
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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