A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13038334



Internal ID2494775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156145763..156147564hg38UCSC Ensembl
Innerchr7:156145790..156147537hg38UCSC Ensembl
Outerchr7:156145736..156147591hg38UCSC Ensembl
chr7:155938457..155940258hg19UCSC Ensembl
Innerchr7:155938484..155940231hg19UCSC Ensembl
Outerchr7:155938430..155940285hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg381802
hg191802
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3615653
Supporting Variants
SamplesHG02215
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13038334
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