A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16319497



Internal ID3578845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36327319..36327848hg38UCSC Ensembl
Innerchr21:36327320..36327848hg38UCSC Ensembl
Outerchr21:36327319..36327849hg38UCSC Ensembl
chr21:37699617..37700146hg19UCSC Ensembl
Innerchr21:37699618..37700146hg19UCSC Ensembl
Outerchr21:37699617..37700147hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38530
hg19530
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3646969
Supporting Variants
SamplesHG03166
Known GenesMORC3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16319497
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