A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1677986



Internal ID12494419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180615577..180615577hg38UCSC Ensembl
chr5:180042577..180042577hg19UCSC Ensembl
chr5:179975183..179975183hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38605
hg19605
hg18605
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4033612
SamplesHuRef
Known GenesFLT4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1677986
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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