A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034916



Internal ID20601956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31883601..31885700hg38UCSC Ensembl
chr17:30210620..30212719hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496185
Supporting Variants
Samples
Known GenesUTP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034916
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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