A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534989



Internal ID20908350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62891058..62895970hg38UCSC Ensembl
chr17:60968419..60973331hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg384913
hg194913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037197
Samples
Known GenesMIR548W
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534989
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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