A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434259



Internal ID21091812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139230301..139232500hg38UCSC Ensembl
chr7:138915047..138917246hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236286
Samples
Known GenesUBN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434259
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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