A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341220



Internal ID20998773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:98971160..99069498hg38UCSC Ensembl
chr2:99587623..99685961hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3898339
hg1998339
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208845
Samples
Known GenesTSGA10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341220
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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