A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13038320



Internal ID425464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156126614..156127065hg38UCSC Ensembl
Innerchr7:156126619..156127061hg38UCSC Ensembl
Outerchr7:156126610..156127070hg38UCSC Ensembl
chr7:155919308..155919759hg19UCSC Ensembl
Innerchr7:155919313..155919755hg19UCSC Ensembl
Outerchr7:155919304..155919764hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38452
hg19452
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3615651
Supporting Variants
SamplesHG00129
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13038320
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