A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037059



Internal ID20604099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57376966..57378340hg38UCSC Ensembl
chr17:55454327..55455701hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg381375
hg191375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6525054
Supporting Variants
Samples
Known GenesMSI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037059
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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