A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15274264



Internal ID1610818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66739716..66763666hg38UCSC Ensembl
chr15:67032054..67056004hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3823951
hg1923951
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636773
Supporting Variants
SamplesHG01494
Known GenesSMAD6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15274264
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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