A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6237544



Internal ID9563164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5872853..5874108hg38UCSC Ensembl
Outerchr10:5872816..5874158hg38UCSC Ensembl
Innerchr10:5914816..5916071hg19UCSC Ensembl
Outerchr10:5914779..5916121hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381343
hg191343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2668731
Supporting Variants
SamplesNA19107
Known GenesANKRD16
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6237544
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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