A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506857



Internal ID20880143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39062481..39070926hg38UCSC Ensembl
chr17:37218734..37227179hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg388446
hg198446
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185506
Samples
Known GenesLOC100131347, PLXDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506857
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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