A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3342969



Internal ID15189954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72233519..72233538hg38UCSC Ensembl
Innerchr10:72233515..72233542hg38UCSC Ensembl
Outerchr10:72233496..72233561hg38UCSC Ensembl
chr10:73993277..73993296hg19UCSC Ensembl
Innerchr10:73993273..73993300hg19UCSC Ensembl
Outerchr10:73993254..73993319hg19UCSC Ensembl
chr10:73663283..73663302hg18UCSC Ensembl
Innerchr10:73663306..73663279hg18UCSC Ensembl
Outerchr10:73663260..73663325hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9648524
SamplesNA12815
Known GenesANAPC16
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3342969
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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