A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429717



Internal ID21087270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:136283162..136303688hg38UCSC Ensembl
chr7:135967910..135988436hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3820527
hg1920527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154336
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429717
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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