A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4144841



Internal ID11080693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89879619..89879871hg38UCSC Ensembl
chr16:89946027..89946279hg19UCSC Ensembl
chr16:88473528..88473780hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38253
hg19253
hg18253
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1404867
Supporting Variants
SamplesHuRef
Known GenesTCF25
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4144841
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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