A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3803457



Internal ID11958414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:38861965..38862160hg38UCSC Ensembl
chr5:38862067..38862262hg19UCSC Ensembl
chr5:38897824..38898019hg18UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38196
hg19196
hg18196
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1589521
Supporting Variants
SamplesHuRef
Known GenesOSMR
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3803457
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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