A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196728



Internal ID20763768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32033052..32034431hg38UCSC Ensembl
chr17:30360071..30361450hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg381380
hg191380
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507621
Supporting Variants
Samples
Known GenesLRRC37B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196728
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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