A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348922



Internal ID21006475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5667001..5715800hg38UCSC Ensembl
chr2:5807133..5855932hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg3848800
hg1948800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206312
Samples
Known GenesSOX11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348922
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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