A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502917



Internal ID20876166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28650846..28651101hg38UCSC Ensembl
chr17:26977864..26978119hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178406
Samples
Known GenesSDF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502917
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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