A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515191



Internal ID20888550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:12215131..12216271hg38UCSC Ensembl
chr17:12118448..12119588hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg381141
hg191141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034164
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515191
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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