A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3451385



Internal ID15298331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72345627..72345655hg38UCSC Ensembl
Innerchr9:72345625..72345655hg38UCSC Ensembl
Outerchr9:72345599..72345683hg38UCSC Ensembl
chr9:74960543..74960571hg19UCSC Ensembl
Innerchr9:74960541..74960571hg19UCSC Ensembl
Outerchr9:74960515..74960599hg19UCSC Ensembl
chr9:74150363..74150391hg18UCSC Ensembl
Innerchr9:74150391..74150361hg18UCSC Ensembl
Outerchr9:74150335..74150419hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38234
hg19234
hg18234
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8677429
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3451385
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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