A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6285994



Internal ID9748729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84945839..84953524hg38UCSC Ensembl
Outerchr15:84945802..84953574hg38UCSC Ensembl
Innerchr15:85489070..85496755hg19UCSC Ensembl
Outerchr15:85489033..85496805hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg387773
hg197773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665580
Supporting Variants
SamplesNA19700
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6285994
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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