A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510288



Internal ID20883605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19738090..19741510hg38UCSC Ensembl
chr17:19641403..19644823hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg383421
hg193421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034831
Samples
Known GenesALDH3A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510288
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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