A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426360



Internal ID21083913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145179781..145180334hg38UCSC Ensembl
chr7:144876874..144877427hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153187
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426360
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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