A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610248



Internal ID20983319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81183845..81292586hg38UCSC Ensembl
chr7:80813161..80921902hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38108742
hg19108742
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217814
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610248
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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