A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3939145



Internal ID11822727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56710786..56710862hg38UCSC Ensembl
chr20:55285842..55285918hg19UCSC Ensembl
chr20:54719249..54719325hg18UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3877
hg1977
hg1877
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1701216
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3939145
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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