A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671411



Internal ID9937516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:100022662..100037900hg38UCSC Ensembl
Outerchr3:100022625..100037950hg38UCSC Ensembl
Innerchr3:99741506..99756744hg19UCSC Ensembl
Outerchr3:99741469..99756794hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3815326
hg1915326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5919837
SamplesHG01055
Known GenesCMSS1, FILIP1L
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671411
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