A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954155



Internal ID16956342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:63322398..63328301hg38UCSC Ensembl
Outerchr2:63549533..63555436hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg385904
hg195904
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002946
SamplesBILGI_BIOE
Known GenesWDPCP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954155
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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