A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4211957



Internal ID11494495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:89273961..89274017hg38UCSC Ensembl
chr13:89926215..89926271hg19UCSC Ensembl
chr13:88724216..88724272hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3857
hg1957
hg1857
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1260056
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4211957
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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