A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664338



Internal ID9583757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:3146469..3146865hg38UCSC Ensembl
Outerchr1:3146432..3146915hg38UCSC Ensembl
Innerchr1:3063033..3063429hg19UCSC Ensembl
Outerchr1:3062996..3063479hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38484
hg19484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6381855
SamplesNA12287
Known GenesPRDM16
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664338
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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