A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603957



Internal ID20977028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:85465774..85571990hg38UCSC Ensembl
chr7:85095090..85201306hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38106217
hg19106217
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217447
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603957
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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