A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337529



Internal ID20995082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:141010391..141010658hg38UCSC Ensembl
chr2:141767960..141768227hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18078329
Samples
Known GenesLRP1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337529
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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