A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608542



Internal ID20981613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:68149420..68150470hg38UCSC Ensembl
chr7:67614407..67615457hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg381051
hg191051
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227183
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608542
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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