A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036560



Internal ID20603600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:60636700..60637161hg38UCSC Ensembl
chr17:58714061..58714522hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38462
hg19462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523744
Supporting Variants
Samples
Known GenesPPM1D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036560
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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