A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602099



Internal ID20975170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:19884798..19898386hg38UCSC Ensembl
chr7:19924421..19938009hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3813589
hg1913589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156835
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602099
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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