A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12732083



Internal ID3916239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35783386..35790484hg38UCSC Ensembl
Innerchr7:35783386..35790484hg38UCSC Ensembl
Outerchr7:35783076..35790664hg38UCSC Ensembl
chr7:35822996..35830094hg19UCSC Ensembl
Innerchr7:35822996..35830094hg19UCSC Ensembl
Outerchr7:35822686..35830274hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg387099
hg197099
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3612820
Supporting Variants
SamplesHG03571
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12732083
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