A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346028



Internal ID21003581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:144718201..144719400hg38UCSC Ensembl
chr2:145475768..145476967hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18078159
Samples
Known GenesTEX41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346028
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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