A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6265668



Internal ID9066015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:28131516..28131855hg38UCSC Ensembl
Outerchr1:28131341..28132023hg38UCSC Ensembl
Innerchr1:28458027..28458366hg19UCSC Ensembl
Outerchr1:28457852..28458534hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38683
hg19683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2671570
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6265668
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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