A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18080003



Internal ID20647043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:170192401..170193400hg38UCSC Ensembl
chr2:171048911..171049910hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6354551
Supporting Variants
Samples
Known GenesMYO3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18080003
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00086


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