A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501891



Internal ID20875129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:45279174..45280362hg38UCSC Ensembl
chr17:43356541..43357729hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg381189
hg191189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035900
Samples
Known GenesMAP3K14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501891
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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