A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1242e214



Internal ID22757136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:272004..295089hg38UCSC Ensembl
chr7:311970..335055hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3823086
hg1923086
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3611769, esv3611767
SamplesNA18543, NA18549
Known GenesLOC100288524
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1242e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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