A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618887



Internal ID20991958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21421134..21435213hg38UCSC Ensembl
chr7:21460752..21474831hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3814080
hg1914080
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230784
Samples
Known GenesSP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618887
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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