A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3636179



Internal ID12125689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:6462518..6462584hg38UCSC Ensembl
chr20:6443165..6443231hg19UCSC Ensembl
chr20:6391165..6391231hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3867
hg1967
hg1867
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1510134
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3636179
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer