A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7864948



Internal ID12970942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91906019..91906019hg38UCSC Ensembl
Innerchr9:91906014..91906024hg38UCSC Ensembl
Outerchr9:91906014..91906024hg38UCSC Ensembl
chr9:94668301..94668301hg19UCSC Ensembl
Innerchr9:94668296..94668306hg19UCSC Ensembl
Outerchr9:94668296..94668306hg19UCSC Ensembl
chr9:93708122..93708122hg18UCSC Ensembl
Innerchr9:93708127..93708117hg18UCSC Ensembl
Outerchr9:93708117..93708127hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3855
hg1955
hg1855
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3343493
Supporting Variants
SamplesNA12005
Known GenesROR2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7864948
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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