A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5537090



Internal ID9285132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:48348320..48355855hg38UCSC Ensembl
Outerchr15:48348163..48356008hg38UCSC Ensembl
Innerchr15:48640517..48648052hg19UCSC Ensembl
Outerchr15:48640360..48648205hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg387846
hg197846
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676621
Supporting Variants
SamplesNA12763
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5537090
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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