A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6021159



Internal ID8998562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:30636376..30642399hg38UCSC Ensembl
Outerchr6:30636339..30642449hg38UCSC Ensembl
Innerchr6:30604153..30610176hg19UCSC Ensembl
Outerchr6:30604116..30610226hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg386111
hg196111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677891
Supporting Variants
SamplesNA19920
Known GenesATAT1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6021159
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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