A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380868



Internal ID21038421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:77968002..78733677hg38UCSC Ensembl
chr4:78889156..79654831hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38765676
hg19765676
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212397
Samples
Known GenesANXA3, FRAS1, LINC01094
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380868
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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