A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3993553



Internal ID11768320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96118966..96119018hg38UCSC Ensembl
chr15:96662195..96662247hg19UCSC Ensembl
chr15:94463199..94463251hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3853
hg1953
hg1853
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1270605
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3993553
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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