A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615116



Internal ID7002005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135234558..135235726hg38UCSC Ensembl
Innerchr7:135234568..135235717hg38UCSC Ensembl
Outerchr7:135234549..135235736hg38UCSC Ensembl
chr7:134919310..134920478hg19UCSC Ensembl
Innerchr7:134919320..134920469hg19UCSC Ensembl
Outerchr7:134919301..134920488hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381169
hg191169
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12975955, essv12975954
SamplesNA19375, NA19376
Known GenesSTRA8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615116
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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