A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676301



Internal ID9942406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:9915636..9920052hg38UCSC Ensembl
Outerchr1:9915479..9920205hg38UCSC Ensembl
Innerchr1:9975694..9980110hg19UCSC Ensembl
Outerchr1:9975537..9980263hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg384727
hg194727
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6535570
SamplesHG00607
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676301
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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