A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6370674



Internal ID9459486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29592527..29593769hg38UCSC Ensembl
chr8:29450043..29451285hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381243
hg191243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2672104
Supporting Variants
SamplesNA18909
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6370674
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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