A curated catalogue of human genomic structural variation




Variant Details

Variant: esv994389



Internal ID6730344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78791922..78792013hg38UCSC Ensembl
chr15:79084264..79084355hg19UCSC Ensembl
chr15:76871319..76871410hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3892
hg1992
hg1892
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3579065
SamplesHuRef
Known GenesADAMTS7
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv994389
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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