A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512181



Internal ID20885512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45193053..45195290hg38UCSC Ensembl
chr17:43270420..43272657hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg382238
hg192238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035896
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512181
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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