A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502353



Internal ID20875597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21111202..21303044hg38UCSC Ensembl
chr17:21014515..21206356hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38191843
hg19191842
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188868
Samples
Known GenesC17orf103, DHRS7B, MAP2K3, TMEM11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502353
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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