A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421627



Internal ID21079180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132007176..132007521hg38UCSC Ensembl
chr7:131691935..131692280hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150951
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421627
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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