A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513826



Internal ID20887174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1697163..1708626hg38UCSC Ensembl
chr17:1600457..1611920hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3811464
hg1911464
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191311
Samples
Known GenesTLCD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513826
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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