A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353339



Internal ID21010892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5937292..5942578hg38UCSC Ensembl
chr2:6077424..6082710hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg385287
hg195287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088741
Samples
Known GenesLINC01105
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353339
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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