A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6118952



Internal ID9096355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:91913633..91916801hg38UCSC Ensembl
Outerchr9:91913476..91916954hg38UCSC Ensembl
Innerchr9:94675915..94679083hg19UCSC Ensembl
Outerchr9:94675758..94679236hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg383479
hg193479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663538
Supporting Variants
SamplesHG00247
Known GenesROR2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6118952
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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