A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12199814



Internal ID2278345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14935197..14941140hg38UCSC Ensembl
Innerchr6:14935347..14940990hg38UCSC Ensembl
Outerchr6:14935047..14941290hg38UCSC Ensembl
chr6:14935428..14941371hg19UCSC Ensembl
Innerchr6:14935578..14941221hg19UCSC Ensembl
Outerchr6:14935278..14941521hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg385944
hg195944
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3608157
Supporting Variants
SamplesHG02032
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12199814
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