A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15256388



Internal ID4596634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55986870..56021506hg38UCSC Ensembl
chr15:56279068..56313704hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3834637
hg1934637
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636573
Supporting Variants
SamplesHG04107
Known GenesNEDD4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15256388
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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