A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636429



Internal ID7023223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49511894..49538855hg38UCSC Ensembl
Innerchr15:49512044..49538705hg38UCSC Ensembl
Outerchr15:49511744..49539005hg38UCSC Ensembl
chr15:49804091..49831052hg19UCSC Ensembl
Innerchr15:49804241..49830902hg19UCSC Ensembl
Outerchr15:49803941..49831202hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3826962
hg1926962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15245740
SamplesHG01965
Known GenesFAM227B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636429
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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