A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5629851



Internal ID9423772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130277818..130277918hg38UCSC Ensembl
Outerchr9:130277781..130277968hg38UCSC Ensembl
Innerchr9:133040097..133040197hg19UCSC Ensembl
Outerchr9:133040060..133040247hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38188
hg19188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2663591
Supporting Variants
SamplesNA18623
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5629851
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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