A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3588786



Internal ID12173082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89994517..89994517hg38UCSC Ensembl
chr8:91006745..91006745hg19UCSC Ensembl
chr8:91075921..91075921hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38137
hg19137
hg18137
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1748740
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3588786
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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