A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12710379



Internal ID5704492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26213912..26214942hg19UCSC Ensembl
Innerchr7:26213952..26214902hg19UCSC Ensembl
Outerchr7:26213872..26214982hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg381031
hg19n/a
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3612627
Supporting Variants
SamplesNA19090
Known GenesNFE2L3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12710379
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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