A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608345



Internal ID20981416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73544944..73552087hg38UCSC Ensembl
chr7:72959274..72966417hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg387144
hg197144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159454
Samples
Known GenesBCL7B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608345
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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