A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528369



Internal ID20901730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81809211..81809586hg38UCSC Ensembl
chr17:79767087..79767462hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38376
hg19376
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181908
Samples
Known GenesGCGR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528369
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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