A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3709004



Internal ID12052866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8655150..8655251hg38UCSC Ensembl
chr3:8696836..8696937hg19UCSC Ensembl
chr3:8671836..8671937hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38102
hg19102
hg18102
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1225869
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3709004
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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