A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341845



Internal ID20999398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:104395398..104398725hg38UCSC Ensembl
chr2:105011856..105015183hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg383328
hg193328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18076595
Samples
Known GenesLOC100287010
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341845
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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