A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035672



Internal ID20602712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42992215..42995853hg38UCSC Ensembl
chr17:41144232..41147870hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg383639
hg193639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497294
Supporting Variants
Samples
Known GenesRUNDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035672
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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