A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035599



Internal ID20602639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:33126772..33127133hg38UCSC Ensembl
chr17:31453790..31454151hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38362
hg19362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497245
Supporting Variants
Samples
Known GenesASIC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035599
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00676


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