A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350168



Internal ID21007721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:104457701..104459200hg38UCSC Ensembl
chr2:105074159..105075658hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18076597
Samples
Known GenesLINC01102
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350168
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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