A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602900



Internal ID20975971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:68467124..68477652hg38UCSC Ensembl
chr7:67932111..67942639hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3810529
hg1910529
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231733
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602900
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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