A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6448599



Internal ID9426002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:107284276..107291102hg38UCSC Ensembl
Outerchr9:107284239..107291152hg38UCSC Ensembl
Innerchr9:110046557..110053383hg19UCSC Ensembl
Outerchr9:110046520..110053433hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg386914
hg196914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669320
Supporting Variants
SamplesHG01047
Known GenesRAD23B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6448599
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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