A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1628034



Internal ID12444468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63552102..63552102hg38UCSC Ensembl
chr2:63779236..63779236hg19UCSC Ensembl
chr2:63632740..63632740hg18UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38327
hg19327
hg18327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3890229
SamplesHuRef
Known GenesWDPCP
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1628034
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