A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612846



Internal ID20985917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93226784..93227456hg38UCSC Ensembl
chr7:92856097..92856769hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38673
hg19673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161758
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612846
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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