A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523651



Internal ID20897012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:51290275..51291509hg38UCSC Ensembl
chr17:49367636..49368870hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg381235
hg191235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036849
Samples
Known GenesUTP18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523651
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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