A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637265



Internal ID6677372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92583664..92605084hg38UCSC Ensembl
chr15:93126894..93148314hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3821421
hg1921421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv461e214
Supporting Variantsessv15320970, essv15320969
SamplesNA20911, HG01597
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637265
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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