A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659119



Internal ID2892206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16208013..16291287hg38UCSC Ensembl
Outerchr7:16207976..16291337hg38UCSC Ensembl
Innerchr7:16247638..16330912hg19UCSC Ensembl
Outerchr7:16247601..16330962hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3883362
hg1983362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5461504
SamplesNA18621
Known GenesISPD, ISPD-AS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659119
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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