A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3763769



Internal ID11651415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89421265..89421415hg38UCSC Ensembl
chr16:89487673..89487823hg19UCSC Ensembl
chr16:88015174..88015324hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38151
hg19151
hg18151
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1506985
Supporting Variants
SamplesHuRef
Known GenesANKRD11
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3763769
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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