A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15385631



Internal ID5387447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15576113..15580633hg38UCSC Ensembl
Innerchr16:15576163..15580583hg38UCSC Ensembl
Outerchr16:15576063..15580683hg38UCSC Ensembl
chr16:15669970..15674490hg19UCSC Ensembl
Innerchr16:15670020..15674440hg19UCSC Ensembl
Outerchr16:15669920..15674540hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg384521
hg194521
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638037
Supporting Variants
SamplesHG02088
Known GenesC16orf45
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15385631
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