A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034255



Internal ID20601295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:2062792..2063662hg38UCSC Ensembl
chr17:1966086..1966956hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38871
hg19871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499904
Supporting Variants
Samples
Known GenesSMG6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034255
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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