A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4232372



Internal ID11514910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105831020..105831153hg38UCSC Ensembl
chr6:106278895..106279028hg19UCSC Ensembl
chr6:106385588..106385721hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38134
hg19134
hg18134
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1575076
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4232372
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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