A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv948e214



Internal ID22756842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160177597..160182076hg38UCSC Ensembl
chr3:159895384..159899863hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg384480
hg194480
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3598379, esv3598380
SamplesHG02471, NA19347, NA19327, NA19452, NA19436, HG02759, HG03469, NA19376, HG03166
Known GenesIL12A-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv948e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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