A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615157



Internal ID7002046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:136839736..136854545hg38UCSC Ensembl
Innerchr7:136839766..136854516hg38UCSC Ensembl
Outerchr7:136839707..136854575hg38UCSC Ensembl
chr7:136524483..136539292hg19UCSC Ensembl
Innerchr7:136524513..136539263hg19UCSC Ensembl
Outerchr7:136524454..136539322hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3814810
hg1914810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12979493, essv12979494
SamplesNA19072, HG01874
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615157
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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