A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513637



Internal ID20886983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15332720..15333232hg38UCSC Ensembl
chr17:15236037..15236549hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033890
Samples
Known GenesTEKT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513637
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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