A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3730789



Internal ID11684395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:90008190..90008352hg38UCSC Ensembl
chr16:90074598..90074760hg19UCSC Ensembl
chr16:88602099..88602261hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38163
hg19163
hg18163
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1095561
Supporting Variants
SamplesHuRef
Known GenesDBNDD1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3730789
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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