A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340786



Internal ID20998339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:229398001..229399800hg38UCSC Ensembl
chr2:230262717..230264516hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084795
Samples
Known GenesDNER
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340786
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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