A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5719707



Internal ID8854434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:37097615..37102321hg38UCSC Ensembl
Outerchr15:37097244..37102791hg38UCSC Ensembl
Innerchr15:37389816..37394522hg19UCSC Ensembl
Outerchr15:37389445..37394992hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg385548
hg195548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676776
Supporting Variants
SamplesHG00310
Known GenesMEIS2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5719707
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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