A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034770



Internal ID20601810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18905140..18906332hg38UCSC Ensembl
chr17:18808453..18809645hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381193
hg191193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501853
Supporting Variants
Samples
Known GenesPRPSAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034770
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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