A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355250



Internal ID21012803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:162358201..162360800hg38UCSC Ensembl
chr2:163214711..163217310hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080188
Samples
Known GenesGCA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355250
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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