A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15320967



Internal ID5322783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92497399..92580554hg38UCSC Ensembl
chr15:93040629..93123784hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3883156
hg1983156
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637264
Supporting Variants
SamplesHG01597
Known GenesC15orf32, LINC00930
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15320967
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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