A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615626



Internal ID7002515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155225987..155227275hg38UCSC Ensembl
Innerchr7:155225987..155227275hg38UCSC Ensembl
Outerchr7:155225673..155227586hg38UCSC Ensembl
chr7:155017697..155018985hg19UCSC Ensembl
Innerchr7:155017697..155018985hg19UCSC Ensembl
Outerchr7:155017383..155019296hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg381289
hg191289
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13033261, essv13033262, essv13033260
SamplesNA19701, NA19704, HG01082
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615626
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