A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418871



Internal ID21076424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:133591468..133670968hg38UCSC Ensembl
chr7:133276222..133355721hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3879501
hg1979500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225758
Samples
Known GenesEXOC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418871
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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