A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1768316



Internal ID12584748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83658396..83658978hg38UCSC Ensembl
chr16:83692001..83692583hg19UCSC Ensembl
chr16:82249502..82250084hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38583
hg19583
hg18583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3844800
SamplesHuRef
Known GenesCDH13
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1768316
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer