A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036594



Internal ID20603634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:47900541..47903695hg38UCSC Ensembl
chr17:45977907..45981061hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg383155
hg193155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515740
Supporting Variants
Samples
Known GenesLOC100506325, SP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036594
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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