A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355483



Internal ID21013036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191672201..191684200hg38UCSC Ensembl
chr2:192536927..192548926hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg3812000
hg1912000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205438
Samples
Known GenesNABP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355483
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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