A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377457



Internal ID21035010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:148287337..148418743hg38UCSC Ensembl
chr4:149208489..149339895hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38131407
hg19131407
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212043
Samples
Known GenesNR3C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377457
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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