A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3902549



Internal ID11859322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38807099..38807453hg38UCSC Ensembl
chr22:39203104..39203458hg19UCSC Ensembl
chr22:37533050..37533404hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38355
hg19355
hg18355
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1574182
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3902549
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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