A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036313



Internal ID20603353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58647945..58689459hg38UCSC Ensembl
chr17:56725306..56766820hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3841515
hg1941515
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526500
Supporting Variants
Samples
Known GenesTEX14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036313
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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