A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509606



Internal ID20882917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6760087..6760892hg38UCSC Ensembl
chr17:6663406..6664211hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38806
hg19806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037415
Samples
Known GenesXAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509606
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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