A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354555



Internal ID21012108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:104454901..104456500hg38UCSC Ensembl
chr2:105071359..105072958hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18076596
Samples
Known GenesLINC01102
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354555
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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