A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5712806



Internal ID9264707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:17110540..17112523hg38UCSC Ensembl
Outerchr6:17110503..17112573hg38UCSC Ensembl
Innerchr6:17110771..17112754hg19UCSC Ensembl
Outerchr6:17110734..17112804hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382071
hg192071
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664889
Supporting Variants
SamplesNA12340
Known GenesSTMND1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5712806
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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