A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4033612



Internal ID11381576
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1677986
Supporting Variants
SamplesHuRef
Known GenesFLT4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4033612
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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