A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677825



Internal ID9943930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:91901718..91903400hg38UCSC Ensembl
Outerchr7:91901681..91903450hg38UCSC Ensembl
Innerchr7:91531032..91532714hg19UCSC Ensembl
Outerchr7:91530995..91532764hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg381770
hg191770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6176392, essv5672346
SamplesNA19448, NA18499
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677825
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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