A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2731526



Internal ID5042258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:6261891..6262022hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsessv6963579, essv6956855, essv6860702, essv6670984, essv6865469, essv6848978
SamplesSSM027, SSM086, SSM088, SSM089, SSM031, SSM026
Known GenesF13A1
Method
Analysis
PlatformIllumina HiSeq2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)esv2731526
Frequency
Sample Size96
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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