A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614450



Internal ID7001344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106793452..106794880hg38UCSC Ensembl
Innerchr7:106793509..106794824hg38UCSC Ensembl
Outerchr7:106793396..106794937hg38UCSC Ensembl
chr7:106433898..106435326hg19UCSC Ensembl
Innerchr7:106433955..106435270hg19UCSC Ensembl
Outerchr7:106433842..106435383hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg381429
hg191429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12917664, essv12917663
SamplesNA19713, HG00437
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614450
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer