A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506455



Internal ID20879735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45952368..45955384hg38UCSC Ensembl
chr17:44029734..44032750hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg383017
hg193017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035924
Samples
Known GenesMAPT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506455
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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