A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519563



Internal ID20892924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62740166..62742380hg38UCSC Ensembl
chr17:60817527..60819741hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg382215
hg192215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037193
Samples
Known GenesMARCH10, MIR548W
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519563
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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