A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611854



Internal ID6652069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2830578..2832314hg38UCSC Ensembl
Innerchr7:2830594..2832299hg38UCSC Ensembl
Outerchr7:2830563..2832330hg38UCSC Ensembl
chr7:2870212..2871948hg19UCSC Ensembl
Innerchr7:2870228..2871933hg19UCSC Ensembl
Outerchr7:2870197..2871964hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg381737
hg191737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12668863
SamplesHG01500
Known GenesGNA12
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611854
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