A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612939



Internal ID6999838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:41091254..41094925hg38UCSC Ensembl
Innerchr7:41091754..41094425hg38UCSC Ensembl
Outerchr7:41090254..41095925hg38UCSC Ensembl
chr7:41130852..41134523hg19UCSC Ensembl
Innerchr7:41131352..41134023hg19UCSC Ensembl
Outerchr7:41129852..41135523hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg383672
hg193672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12751922
SamplesHG03731
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612939
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