A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618451



Internal ID20991522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:116667301..116674900hg38UCSC Ensembl
chr7:116307355..116314954hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg387600
hg197600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232442
Samples
Known GenesMET
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618451
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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