A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602097



Internal ID20975168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:6851101..7014000hg38UCSC Ensembl
chr7:6890732..7053631hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38162900
hg19162900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6558n223
Supporting Variantsnssv18230178
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602097
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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