A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670907



Internal ID9937012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39545537..39547091hg38UCSC Ensembl
chr15:39837738..39839292hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381555
hg191555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6435178, essv6515184
SamplesNA18541, NA18542
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670907
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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