A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5740216



Internal ID8894033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:55214145..55215627hg38UCSC Ensembl
Outerchr15:55214108..55215677hg38UCSC Ensembl
Innerchr15:55506343..55507825hg19UCSC Ensembl
Outerchr15:55506306..55507875hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381570
hg191570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2666165
Supporting Variants
SamplesHG00343
Known GenesRAB27A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5740216
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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