A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7833017



Internal ID14832685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88230884..88230885hg38UCSC Ensembl
Innerchr9:88230867..88230902hg38UCSC Ensembl
Outerchr9:88230866..88230903hg38UCSC Ensembl
chr9:90845799..90845800hg19UCSC Ensembl
Innerchr9:90845782..90845817hg19UCSC Ensembl
Outerchr9:90845781..90845818hg19UCSC Ensembl
chr9:90035619..90035620hg18UCSC Ensembl
Innerchr9:90035637..90035602hg18UCSC Ensembl
Outerchr9:90035601..90035638hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38141
hg19141
hg18141
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3306394
Supporting Variants
SamplesNA19099
Known Genes
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7833017
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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