A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035266



Internal ID20602306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38338019..38346975hg38UCSC Ensembl
chr17:36493902..36502857hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg388957
hg198956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504207
Supporting Variants
Samples
Known GenesGPR179
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035266
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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