A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6422796



Internal ID9118894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77479680..77482827hg38UCSC Ensembl
chr15:77772022..77775169hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg383148
hg193148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2660058
Supporting Variants
SamplesHG01133
Known GenesHMG20A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6422796
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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