A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv703e214



Internal ID22756597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62507583..62534329hg38UCSC Ensembl
chr2:62734718..62761464hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3826747
hg1926747
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3591042, esv3591041
SamplesNA19355, NA19437, NA19449, NA19338, NA19321, NA19473, NA19351, NA19431
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv703e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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