A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6260201



Internal ID9188160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168209027..168211003hg38UCSC Ensembl
chr1:168178265..168180241hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg381977
hg191977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677411
Supporting Variants
SamplesHG01462
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6260201
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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