A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036099



Internal ID20603139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:49013301..49015900hg38UCSC Ensembl
chr17:47090663..47093262hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529505
Supporting Variants
Samples
Known GenesIGF2BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036099
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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