A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3851952



Internal ID11909919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70585510..70585751hg38UCSC Ensembl
chr15:70877849..70878090hg19UCSC Ensembl
chr15:68664903..68665144hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38242
hg19242
hg18242
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1401879
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3851952
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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