A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3919626



Internal ID11842245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95079909..95079962hg38UCSC Ensembl
chr8:96092137..96092190hg19UCSC Ensembl
chr8:96161313..96161366hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3854
hg1954
hg1854
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1385707
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3919626
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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