A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15385525



Internal ID5387341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15031082..15082591hg38UCSC Ensembl
chr16:15124939..15176448hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3851510
hg1951510
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638021
Supporting Variants
SamplesHG00334
Known GenesNTAN1, PDXDC1, RRN3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15385525
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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