A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12875152



Internal ID5996785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:84287237..84306398hg38UCSC Ensembl
Innerchr7:84287278..84306357hg38UCSC Ensembl
Outerchr7:84287196..84306439hg38UCSC Ensembl
chr7:83916553..83935714hg19UCSC Ensembl
Innerchr7:83916594..83935673hg19UCSC Ensembl
Outerchr7:83916512..83935755hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3819162
hg1919162
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3613962
Supporting Variants
SamplesNA19397
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12875152
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