A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638022



Internal ID6678120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15031773..15047500hg38UCSC Ensembl
chr16:15125630..15141357hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3815728
hg1915728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15385527, essv15385528
SamplesHG00766, HG01464
Known GenesNTAN1, PDXDC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638022
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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