A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3710829



Internal ID11704355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:17132538..17132593hg38UCSC Ensembl
chr16:17226395..17226450hg19UCSC Ensembl
chr16:17133896..17133951hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3856
hg1956
hg1856
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1343982
Supporting Variants
SamplesHuRef
Known GenesXYLT1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3710829
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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