A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510786



Internal ID20884109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5117996..5118326hg38UCSC Ensembl
chr17:5021291..5021621hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036844
Samples
Known GenesZNF232
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510786
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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