A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602198



Internal ID20975269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16484841..16486016hg38UCSC Ensembl
chr7:16524466..16525641hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg381176
hg191176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152303
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602198
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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