A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12698571



Internal ID1063057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22407079..22414064hg38UCSC Ensembl
Innerchr7:22407098..22414045hg38UCSC Ensembl
Outerchr7:22407060..22414083hg38UCSC Ensembl
chr7:22446698..22453683hg19UCSC Ensembl
Innerchr7:22446717..22453664hg19UCSC Ensembl
Outerchr7:22446679..22453702hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg386986
hg196986
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3612519
Supporting Variants
SamplesHG00689
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12698571
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