A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337798



Internal ID20995351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:211319126..211450018hg38UCSC Ensembl
chr2:212183851..212314743hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38130893
hg19130893
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208133
Samples
Known GenesERBB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337798
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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