A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502271



Internal ID20875514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37565001..37566600hg38UCSC Ensembl
chr17:35925104..35926702hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381600
hg191599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186744
Samples
Known GenesSYNRG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502271
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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