A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1089006



Internal ID11905444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:32949954..32950080hg38UCSC Ensembl
chr15:33242155..33242281hg19UCSC Ensembl
chr15:31029447..31029573hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38127
hg19127
hg18127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4197050
SamplesHuRef
Known GenesFMN1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1089006
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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