A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12974994



Internal ID5161017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134629056..134640671hg38UCSC Ensembl
Innerchr7:134629056..134640671hg38UCSC Ensembl
Outerchr7:134628814..134640932hg38UCSC Ensembl
chr7:134313808..134325423hg19UCSC Ensembl
Innerchr7:134313808..134325423hg19UCSC Ensembl
Outerchr7:134313566..134325684hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3811616
hg1911616
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3615100
Supporting Variants
SamplesNA18593
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12974994
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