A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6429573



Internal ID9690052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:67172612..67173698hg38UCSC Ensembl
chr8:68084847..68085933hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg381087
hg191087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675478
Supporting Variants
SamplesNA19440
Known GenesCSPP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6429573
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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