A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609803



Internal ID20982874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121498597..121499015hg38UCSC Ensembl
chr7:121138651..121139069hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151776
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609803
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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