A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609046



Internal ID20982117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:9265421..9286705hg38UCSC Ensembl
chr7:9305051..9326335hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3821285
hg1921285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18160617
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609046
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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