A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519008



Internal ID20892369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57211249..57211501hg38UCSC Ensembl
chr17:55288610..55288862hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38253
hg19253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037054
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519008
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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