A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3766586



Internal ID11995285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38923746..38923795hg38UCSC Ensembl
chr22:39319751..39319800hg19UCSC Ensembl
chr22:37649697..37649746hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1035522
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3766586
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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