A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4139990



Internal ID11075842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:19234238..19234363hg38UCSC Ensembl
chr8:19091748..19091873hg19UCSC Ensembl
chr8:19136028..19136153hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38126
hg19126
hg18126
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1074859
Supporting Variants
SamplesHuRef
Known GenesLOC100128993
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4139990
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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