A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358127



Internal ID21015680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7711888..7712991hg38UCSC Ensembl
chr4:7713615..7714718hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg381104
hg191104
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212389
Samples
Known GenesSORCS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358127
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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