A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189155



Internal ID20756195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7971253..8065660hg38UCSC Ensembl
chr17:7874571..7968978hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3894408
hg1994408
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508829
Supporting Variants
Samples
Known GenesALOX15B, GUCY2D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189155
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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