A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418430



Internal ID21075983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134882294..134883970hg38UCSC Ensembl
chr7:134567045..134568721hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381677
hg191677
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225631
Samples
Known GenesCALD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418430
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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