A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612810



Internal ID6999710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35099400..35153502hg38UCSC Ensembl
Innerchr7:35099400..35153502hg38UCSC Ensembl
Outerchr7:35098900..35154002hg38UCSC Ensembl
chr7:35139012..35193114hg19UCSC Ensembl
Innerchr7:35139012..35193114hg19UCSC Ensembl
Outerchr7:35138512..35193614hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3854103
hg1954103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12726983, essv12726982, essv12726981
SamplesHG03577, NA20785, HG03469
Known GenesDPY19L2P1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612810
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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