A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355380



Internal ID21012933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:141845301..141849500hg38UCSC Ensembl
chr2:142602870..142607069hg19UCSC Ensembl
Cytoband2q22.2
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4142n223
Supporting Variantsnssv18078703
Samples
Known GenesLRP1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355380
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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