A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1621359



Internal ID12437793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76019533..76019533hg38UCSC Ensembl
chr4:76940686..76940686hg19UCSC Ensembl
chr4:77159710..77159710hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38158
hg19158
hg18158
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3679016
SamplesHuRef
Known GenesART3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1621359
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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