A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533485



Internal ID20906846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77917728..77919551hg38UCSC Ensembl
chr17:75913810..75915633hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg381824
hg191824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039053
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533485
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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