A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15249999



Internal ID6348203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53557180..53595324hg38UCSC Ensembl
chr15:53849377..53887521hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3838145
hg1938145
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636510
Supporting Variants
SamplesNA20276
Known GenesWDR72
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15249999
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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