A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4141160



Internal ID11077012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87726223..87726488hg38UCSC Ensembl
chr16:87759829..87760094hg19UCSC Ensembl
chr16:86317330..86317595hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38266
hg19266
hg18266
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1590350
Supporting Variants
SamplesHuRef
Known GenesKLHDC4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4141160
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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