A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669187



Internal ID9935292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:92522763..92544719hg38UCSC Ensembl
Outerchr13:92522392..92545089hg38UCSC Ensembl
Innerchr13:93175016..93196972hg19UCSC Ensembl
Outerchr13:93174645..93197342hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3822698
hg1922698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5810245, essv6009004, essv5769815
SamplesNA19057, NA18984, NA19004
Known GenesGPC5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669187
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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