A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420560



Internal ID21078113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156595901..156619800hg38UCSC Ensembl
chr7:156388595..156412494hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3823900
hg1923900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219860
Samples
Known GenesLINC01006
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420560
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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