A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503351



Internal ID20876605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10491001..10492100hg38UCSC Ensembl
chr17:10394318..10395417hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034032
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503351
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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