A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606471



Internal ID20979542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66078945..66102377hg38UCSC Ensembl
chr7:65543932..65567364hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3823433
hg1923433
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227465
Samples
Known GenesASL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606471
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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