A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6210549



Internal ID9705888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:201914924..201915587hg38UCSC Ensembl
Outerchr2:201914887..201915637hg38UCSC Ensembl
Innerchr2:202779647..202780310hg19UCSC Ensembl
Outerchr2:202779610..202780360hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38751
hg19751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670329
Supporting Variants
SamplesNA19456
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6210549
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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