A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615049



Internal ID7001938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131907410..131912080hg38UCSC Ensembl
Innerchr7:131907412..131912079hg38UCSC Ensembl
Outerchr7:131907409..131912082hg38UCSC Ensembl
chr7:131592169..131596839hg19UCSC Ensembl
Innerchr7:131592171..131596838hg19UCSC Ensembl
Outerchr7:131592168..131596841hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg384671
hg194671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12972729, essv12972730, essv12972723, essv12972726, essv12972724, essv12972725, essv12972728, essv12972727, essv12972722
SamplesNA21097, HG02661, HG03235, HG04182, HG04214, HG03910, HG02725, HG04099, HG03615
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615049
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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