A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346741



Internal ID21004294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:212216072..212314868hg38UCSC Ensembl
chr2:213080797..213179593hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3898797
hg1998797
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208141
Samples
Known GenesERBB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346741
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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