A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533176



Internal ID20906537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:49218151..49220089hg38UCSC Ensembl
chr17:47295513..47297451hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg381939
hg191939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036112
Samples
Known GenesABI3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533176
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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