A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389655



Internal ID21047208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:81374301..81722900hg38UCSC Ensembl
chr4:82295455..82644054hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg38348600
hg19348600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214697
Samples
Known GenesRASGEF1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389655
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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