A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530843



Internal ID20904204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76735301..77145300hg38UCSC Ensembl
chr17:74731383..75141382hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38410000
hg19410000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178859
Samples
Known GenesLINC00338, MFSD11, MGAT5B, MIR636, MIR6516, SCARNA16, SEC14L1, SRSF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530843
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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