A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621660



Internal ID7008528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121173658..121174672hg38UCSC Ensembl
Innerchr9:121173687..121174643hg38UCSC Ensembl
Outerchr9:121173629..121174701hg38UCSC Ensembl
chr9:123935936..123936950hg19UCSC Ensembl
Innerchr9:123935965..123936921hg19UCSC Ensembl
Outerchr9:123935907..123936979hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg381015
hg191015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13615203
SamplesNA07056
Known GenesCNTRL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621660
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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