A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1631884



Internal ID12795004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95080203..95080506hg38UCSC Ensembl
chr8:96092431..96092734hg19UCSC Ensembl
chr8:96161607..96161910hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38304
hg19304
hg18304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4043905
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1631884
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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