A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6138421



Internal ID9115824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33103779..33106162hg38UCSC Ensembl
Outerchr9:33103742..33106212hg38UCSC Ensembl
Innerchr9:33103777..33106160hg19UCSC Ensembl
Outerchr9:33103740..33106210hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg382471
hg192471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664830
Supporting Variants
SamplesNA18916
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6138421
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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