A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6075975



Internal ID9053378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:78628933..78631762hg38UCSC Ensembl
Outerchr1:78628775..78631915hg38UCSC Ensembl
Innerchr1:79094618..79097447hg19UCSC Ensembl
Outerchr1:79094460..79097600hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg383141
hg193141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661424
Supporting Variants
SamplesHG01357
Known GenesIFI44L
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6075975
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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