A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416148



Internal ID21073701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138207689..138208388hg38UCSC Ensembl
chr7:137892435..137893134hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155185
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416148
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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