A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615101



Internal ID7001990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134683861..134689586hg38UCSC Ensembl
Innerchr7:134683861..134689586hg38UCSC Ensembl
Outerchr7:134683665..134689803hg38UCSC Ensembl
chr7:134368613..134374338hg19UCSC Ensembl
Innerchr7:134368613..134374338hg19UCSC Ensembl
Outerchr7:134368417..134374555hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg385726
hg195726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12974995
SamplesHG02190
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615101
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