A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675601



Internal ID9941706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:121173761..121174680hg38UCSC Ensembl
Outerchr9:121173724..121174730hg38UCSC Ensembl
Innerchr9:123936039..123936958hg19UCSC Ensembl
Outerchr9:123936002..123937008hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg381007
hg191007
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5429268
SamplesNA07056
Known GenesCNTRL
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675601
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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