A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429811



Internal ID21087364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148699401..148704200hg38UCSC Ensembl
chr7:148396493..148401292hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg384800
hg194800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232205
Samples
Known GenesCUL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429811
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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