A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508642



Internal ID20881946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19668598..19669007hg38UCSC Ensembl
chr17:19571911..19572320hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034825
Samples
Known GenesALDH3A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508642
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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