A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv25e214



Internal ID22755919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:71941634..72011952hg38UCSC Ensembl
chr1:72407317..72477635hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3870319
hg1970319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3586392, esv3586391
SamplesHG04206, HG00683, NA18747
Known GenesNEGR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv25e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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