A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18038056



Internal ID20605096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71976001..71983170hg38UCSC Ensembl
chr17:69972142..69979311hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg387170
hg197170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529016
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18038056
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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