A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207666



Internal ID20774706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:77163635..77220979hg38UCSC Ensembl
chr2:77390761..77448105hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3857345
hg1957345
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6349941
Supporting Variants
Samples
Known GenesLRRTM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207666
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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