A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7837053



Internal ID15038320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17699961..17699962hg38UCSC Ensembl
Innerchr9:17699797..17700126hg38UCSC Ensembl
Outerchr9:17699796..17700127hg38UCSC Ensembl
chr9:17699959..17699960hg19UCSC Ensembl
Innerchr9:17699795..17700124hg19UCSC Ensembl
Outerchr9:17699794..17700125hg19UCSC Ensembl
chr9:17689959..17689960hg18UCSC Ensembl
Innerchr9:17690124..17689795hg18UCSC Ensembl
Outerchr9:17689794..17690125hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3881
hg1981
hg1881
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3308093
Supporting Variants
SamplesNA19239
Known GenesSH3GL2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7837053
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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