A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612331



Internal ID6999232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14996902..15081927hg38UCSC Ensembl
chr7:15036527..15121552hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3885026
hg1985026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12685804, essv12685802, essv12685803
SamplesNA12813, NA19324, NA19429
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612331
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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