A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665672



Internal ID9931777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:97495628..97498197hg38UCSC Ensembl
Outerchr12:97495591..97498247hg38UCSC Ensembl
Innerchr12:97889406..97891975hg19UCSC Ensembl
Outerchr12:97889369..97892025hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg382657
hg192657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6586913
SamplesNA19067
Known GenesRMST
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665672
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