A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429058



Internal ID21086611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137122585..137123023hg38UCSC Ensembl
chr7:136807332..136807770hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38439
hg19439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154436
Samples
Known GenesLOC349160
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429058
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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