A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6170909



Internal ID9148312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:72102253..72106128hg38UCSC Ensembl
Outerchr10:72102096..72106281hg38UCSC Ensembl
Innerchr10:73862011..73865886hg19UCSC Ensembl
Outerchr10:73861854..73866039hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg384186
hg194186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665226
Supporting Variants
SamplesNA18909
Known GenesASCC1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6170909
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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