A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6105693



Internal ID8749509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:103173776..103201278hg38UCSC Ensembl
Outerchr6:103173742..103201313hg38UCSC Ensembl
Innerchr6:103621651..103649153hg19UCSC Ensembl
Outerchr6:103621617..103649188hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3827572
hg1927572
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671762
Supporting Variants
SamplesHG00139
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6105693
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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