A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4222468



Internal ID11158320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77290523..77290999hg38UCSC Ensembl
chr3:77339674..77340150hg19UCSC Ensembl
chr3:77422364..77422840hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38477
hg19477
hg18477
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1228509
Supporting Variants
SamplesHuRef
Known GenesROBO2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4222468
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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