A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1601449



Internal ID12417883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2961235..2961235hg38UCSC Ensembl
chr4:2962962..2962962hg19UCSC Ensembl
chr4:2932760..2932760hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38213
hg19213
hg18213
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3893820
SamplesHuRef
Known GenesNOP14
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1601449
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer