A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3599878



Internal ID11815304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8564856..8564916hg38UCSC Ensembl
chr16:8614858..8614918hg19UCSC Ensembl
chr16:8554859..8554919hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3861
hg1961
hg1861
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1544132
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3599878
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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