A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4215143



Internal ID11497681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90495870..90495972hg38UCSC Ensembl
chr13:91148124..91148226hg19UCSC Ensembl
chr13:89946125..89946227hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38103
hg19103
hg18103
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1425806
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4215143
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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