A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637995



Internal ID7024781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14055686..14063877hg38UCSC Ensembl
Innerchr16:14055686..14063877hg38UCSC Ensembl
Outerchr16:14055447..14064026hg38UCSC Ensembl
chr16:14149543..14157734hg19UCSC Ensembl
Innerchr16:14149543..14157734hg19UCSC Ensembl
Outerchr16:14149304..14157883hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg388192
hg198192
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15378626
SamplesHG02634
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637995
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer