A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341231



Internal ID20998784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:15305754..15306929hg38UCSC Ensembl
chr2:15445878..15447053hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg381176
hg191176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18078955
Samples
Known GenesNBAS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341231
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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