A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506397



Internal ID20879676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17240172..17242976hg38UCSC Ensembl
chr17:17143486..17146290hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg382805
hg192805
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034088
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506397
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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