A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8687937



Internal ID15038935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132573158..132574356hg38UCSC Ensembl
Innerchr10:132573356..132574158hg38UCSC Ensembl
Outerchr10:132572158..132575356hg38UCSC Ensembl
chr10:134386662..134387860hg19UCSC Ensembl
Innerchr10:134386860..134387662hg19UCSC Ensembl
Outerchr10:134385662..134388860hg19UCSC Ensembl
chr10:134236652..134237850hg18UCSC Ensembl
Innerchr10:134237652..134236850hg18UCSC Ensembl
Outerchr10:134235652..134238850hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg381199
hg191199
hg181199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3332310
Supporting Variants
SamplesNA19239
Known GenesINPP5A
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8687937
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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