A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612678



Internal ID6999578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:28910998..28911779hg38UCSC Ensembl
Innerchr7:28911012..28911766hg38UCSC Ensembl
Outerchr7:28910985..28911793hg38UCSC Ensembl
chr7:28950615..28951396hg19UCSC Ensembl
Innerchr7:28950629..28951383hg19UCSC Ensembl
Outerchr7:28950602..28951410hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38782
hg19782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12715689
SamplesHG03099
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612678
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