A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4122277



Internal ID11058130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89907708..89907832hg38UCSC Ensembl
chr16:89974116..89974240hg19UCSC Ensembl
chr16:88501617..88501741hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38125
hg19125
hg18125
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1528431
Supporting Variants
SamplesHuRef
Known GenesTCF25
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4122277
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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