A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5829476



Internal ID9086114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:36158592..36166447hg38UCSC Ensembl
Outerchr1:36158435..36166600hg38UCSC Ensembl
Innerchr1:36624193..36632048hg19UCSC Ensembl
Outerchr1:36624036..36632201hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg388166
hg198166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671242
Supporting Variants
SamplesHG01067
Known GenesMAP7D1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5829476
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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