A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420378



Internal ID21077931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140672601..140674300hg38UCSC Ensembl
chr7:140372401..140374100hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219356
Samples
Known GenesADCK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420378
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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