A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3310305



Internal ID15157256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72345628..72345629hg38UCSC Ensembl
Innerchr9:72345588..72345669hg38UCSC Ensembl
Outerchr9:72345587..72345670hg38UCSC Ensembl
chr9:74960544..74960545hg19UCSC Ensembl
Innerchr9:74960504..74960585hg19UCSC Ensembl
Outerchr9:74960503..74960586hg19UCSC Ensembl
chr9:74150364..74150365hg18UCSC Ensembl
Innerchr9:74150405..74150324hg18UCSC Ensembl
Outerchr9:74150323..74150406hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38137
hg19137
hg18137
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7836676
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3310305
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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