A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677430



Internal ID9943535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42553068..42554533hg38UCSC Ensembl
Outerchr15:42553031..42554583hg38UCSC Ensembl
Innerchr15:42845266..42846731hg19UCSC Ensembl
Outerchr15:42845229..42846781hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg381553
hg191553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6574587
SamplesHG01051
Known GenesHAUS2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677430
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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