A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4248744



Internal ID11184596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15104470..15104541hg38UCSC Ensembl
chr16:15198327..15198398hg19UCSC Ensembl
chr16:15105828..15105899hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3872
hg1972
hg1872
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1168353
Supporting Variants
SamplesHuRef
Known GenesPDXDC1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4248744
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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