A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420812



Internal ID21078365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138418543..138421427hg38UCSC Ensembl
chr7:138103288..138106172hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg382885
hg192885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155207
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420812
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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