A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6115956



Internal ID9689102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158816379..158817518hg38UCSC Ensembl
Outerchr1:158816345..158817553hg38UCSC Ensembl
Innerchr1:158786169..158787308hg19UCSC Ensembl
Outerchr1:158786135..158787343hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg381209
hg191209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666684
Supporting Variants
SamplesNA19439
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6115956
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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