A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502995



Internal ID20876245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45969410..45969642hg38UCSC Ensembl
chr17:44046776..44047008hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035927
Samples
Known GenesMAPT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502995
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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