A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6210507



Internal ID9355734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88833003..89265365hg38UCSC Ensembl
Outerchr2:88832632..89265735hg38UCSC Ensembl
Innerchr2:89132516..89565122hg19UCSC Ensembl
Outerchr2:89132145..89565492hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38433104
hg19433348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656659
Supporting Variants
SamplesNA18550
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6210507
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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