A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6497808



Internal ID9118083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:58808758..58809885hg38UCSC Ensembl
Outerchr15:58808721..58809935hg38UCSC Ensembl
Innerchr15:59100957..59102084hg19UCSC Ensembl
Outerchr15:59100920..59102134hg19UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg381215
hg191215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2656587
Supporting Variants
SamplesHG01125
Known GenesFAM63B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6497808
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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