A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533601



Internal ID20906962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:77799429..77799977hg38UCSC Ensembl
chr17:75795511..75796059hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38549
hg19549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039040
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533601
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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