A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7738203



Internal ID13028228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101419935..101420057hg38UCSC Ensembl
Outerchr9:101419735..101420257hg38UCSC Ensembl
Innerchr9:104182217..104182339hg19UCSC Ensembl
Outerchr9:104182017..104182539hg19UCSC Ensembl
Innerchr9:103222038..103222160hg18UCSC Ensembl
Outerchr9:103221838..103222360hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38523
hg19523
hg18523
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3302700
Supporting Variants
SamplesNA07037
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7738203
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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