A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15501457



Internal ID1009777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67578772..67590885hg38UCSC Ensembl
Innerchr16:67579272..67590385hg38UCSC Ensembl
Outerchr16:67577772..67591885hg38UCSC Ensembl
chr16:67612675..67624788hg19UCSC Ensembl
Innerchr16:67613175..67624288hg19UCSC Ensembl
Outerchr16:67611675..67625788hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3812114
hg1912114
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638890
Supporting Variants
SamplesHG00631
Known GenesCTCF
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15501457
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