A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5672566



Internal ID8927651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:46214406..46216537hg38UCSC Ensembl
Outerchr7:46214249..46216690hg38UCSC Ensembl
Innerchr7:46254004..46256135hg19UCSC Ensembl
Outerchr7:46253847..46256288hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg382442
hg192442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678018
Supporting Variants
SamplesHG00437
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5672566
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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