A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601215



Internal ID20974286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28847101..28855500hg38UCSC Ensembl
chr7:28886718..28895117hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg388400
hg198400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227445
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601215
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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