A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340659



Internal ID20998212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:141407814..141520856hg38UCSC Ensembl
chr2:142165383..142278425hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg38113043
hg19113043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4139n223
Supporting Variantsnssv18078628
Samples
Known GenesLRP1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340659
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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