A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036802



Internal ID20603842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:61000816..61008346hg38UCSC Ensembl
chr17:59078177..59085707hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg387531
hg197531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531348
Supporting Variants
Samples
Known GenesBCAS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036802
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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