A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607618



Internal ID20980689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1269512..1353328hg38UCSC Ensembl
chr7:1309148..1392964hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3883817
hg1983817
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225064
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607618
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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