A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5583786



Internal ID9054740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:32750903..32751073hg38UCSC Ensembl
Outerchr1:32750746..32751226hg38UCSC Ensembl
Innerchr1:33216504..33216674hg19UCSC Ensembl
Outerchr1:33216347..33216827hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2657788
Supporting Variants
SamplesHG00701
Known GenesKIAA1522
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5583786
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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