A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433370



Internal ID21090923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134609851..134684812hg38UCSC Ensembl
chr7:134294603..134369564hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3874962
hg1974962
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236413
Samples
Known GenesBPGM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433370
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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