A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7121135



Internal ID10052731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:17824001..17830001hg38UCSC Ensembl
Innerchr10:17866000..17872000hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2851568
Supporting Variants
SamplesHuRef
Known GenesMRC1
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7121135
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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