A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675581



Internal ID9595000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:9111802..9116208hg38UCSC Ensembl
Outerchr1:9111765..9116258hg38UCSC Ensembl
Innerchr1:9171861..9176267hg19UCSC Ensembl
Outerchr1:9171824..9176317hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg384494
hg194494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6355094
SamplesNA18983
Known GenesGPR157
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675581
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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