A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520355



Internal ID20893716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68055155..68203050hg38UCSC Ensembl
chr17:66051271..66199191hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38147896
hg19147921
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037455
Samples
Known GenesLINC00674, LOC440461
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520355
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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