A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1260056



Internal ID12423179
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2e22
Supporting Variantsessv4211957
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1260056
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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