A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513171



Internal ID20886512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19648004..19660560hg38UCSC Ensembl
chr17:19551317..19563873hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3812557
hg1912557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034823
Samples
Known GenesALDH3A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513171
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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