A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497866



Internal ID20871074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:11546002..11581318hg38UCSC Ensembl
chr17:11449319..11484635hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3835317
hg1935317
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180705
Samples
Known GenesSHISA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497866
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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