A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034566



Internal ID20601606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15788901..15791700hg38UCSC Ensembl
chr17:15692215..15695014hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508132
Supporting Variants
Samples
Known GenesMEIS3P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034566
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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