A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3350656



Internal ID15197637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:62493655..62510853hg38UCSC Ensembl
Innerchr9:62494655..62509853hg38UCSC Ensembl
Outerchr9:62492655..62511853hg38UCSC Ensembl
chr9:46804956..46822154hg19UCSC Ensembl
Innerchr9:46805956..46821154hg19UCSC Ensembl
Outerchr9:46803956..46823154hg19UCSC Ensembl
chr9:46644952..46662150hg18UCSC Ensembl
Innerchr9:46645952..46661150hg18UCSC Ensembl
Outerchr9:46643952..46663150hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3817199
hg1917199
hg1817199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8696990
SamplesNA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3350656
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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