A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3745474



Internal ID12016396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69325428..69325496hg38UCSC Ensembl
chr16:69359331..69359399hg19UCSC Ensembl
chr16:67916832..67916900hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3869
hg1969
hg1869
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1563205
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3745474
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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