A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1500777



Internal ID12317213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:307329..307422hg38UCSC Ensembl
chr5:307444..307537hg19UCSC Ensembl
chr5:360444..360537hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3894
hg1994
hg1894
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3654317
SamplesHuRef
Known GenesAHRR, PDCD6
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1500777
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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