A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12186355



Internal ID5768538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10096821..10105256hg38UCSC Ensembl
Innerchr6:10096842..10105235hg38UCSC Ensembl
Outerchr6:10096800..10105277hg38UCSC Ensembl
chr6:10097054..10105489hg19UCSC Ensembl
Innerchr6:10097075..10105468hg19UCSC Ensembl
Outerchr6:10097033..10105510hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg388436
hg198436
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3608062
Supporting Variants
SamplesNA19138
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12186355
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