A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv460e214



Internal ID20121883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92496954..92603286hg38UCSC Ensembl
chr15:93040184..93146516hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38106333
hg19106333
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3637263, esv3637264
SamplesNA20911, HG01597
Known GenesC15orf32, LINC00930
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv460e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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