A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3960937



Internal ID11454249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106535761..106536080hg38UCSC Ensembl
chr6:106983636..106983955hg19UCSC Ensembl
chr6:107090329..107090648hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38320
hg19320
hg18320
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1180121
Supporting Variants
SamplesHuRef
Known GenesAIM1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3960937
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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