A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5653921



Internal ID8631324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1625736..1635660hg38UCSC Ensembl
Outerchr1:1625365..1636030hg38UCSC Ensembl
Innerchr1:1561116..1571022hg19UCSC Ensembl
Outerchr1:1560745..1571392hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3810666
hg1910648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv2661270
Supporting Variants
SamplesHG00692
Known GenesCDK11B, MIB2, MMP23A, MMP23B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5653921
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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