A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515341



Internal ID20888700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34284091..34287539hg38UCSC Ensembl
chr17:32611110..32614558hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg383449
hg193449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035051
Samples
Known GenesCCL11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515341
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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