A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637900



Internal ID6678000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10448860..10451013hg38UCSC Ensembl
Innerchr16:10448885..10450989hg38UCSC Ensembl
Outerchr16:10448836..10451038hg38UCSC Ensembl
chr16:10542717..10544870hg19UCSC Ensembl
Innerchr16:10542742..10544846hg19UCSC Ensembl
Outerchr16:10542693..10544895hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg382154
hg192154
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15373025, essv15373024
SamplesHG02371, HG03934
Known GenesATF7IP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637900
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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