A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177796



Internal ID20744836
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 StatusS
Merged Variantsnsv6520588
Supporting Variants
Samples
Known GenesJMJD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177796
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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