A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3850853



Internal ID11911018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89745693..89745769hg38UCSC Ensembl
chr16:89812101..89812177hg19UCSC Ensembl
chr16:88339602..88339678hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3877
hg1977
hg1877
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1172602
Supporting Variants
SamplesHuRef
Known GenesFANCA
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3850853
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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