A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509082



Internal ID20882388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32256992..32261873hg38UCSC Ensembl
chr17:30584011..30588892hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg384882
hg194882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034941
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509082
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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