A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3754753



Internal ID12007117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38116159..38116159hg38UCSC Ensembl
chr20:36744561..36744561hg19UCSC Ensembl
chr20:36177975..36177975hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3856
hg1956
hg1856
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1091261
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3754753
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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