A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520588



Internal ID20893949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76723123..76724299hg38UCSC Ensembl
chr17:74719205..74720381hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381177
hg191177
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177796
Samples
Known GenesJMJD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520588
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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