A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3589106



Internal ID11826076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168625505..168625505hg38UCSC Ensembl
chr4:169546656..169546656hg19UCSC Ensembl
chr4:169783231..169783231hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3856
hg1956
hg1856
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1342986
Supporting Variants
SamplesHuRef
Known GenesPALLD
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3589106
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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