A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12890772



Internal ID4340972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93163904..93167560hg38UCSC Ensembl
Innerchr7:93163943..93167521hg38UCSC Ensembl
Outerchr7:93163865..93167599hg38UCSC Ensembl
chr7:92793217..92796873hg19UCSC Ensembl
Innerchr7:92793256..92796834hg19UCSC Ensembl
Outerchr7:92793178..92796912hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg383657
hg193657
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3614156
Supporting Variants
SamplesHG03884
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12890772
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