A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2272



Internal ID15195099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:88795859..88892642hg38UCSC Ensembl
Outerchr2:89095376..89192158hg19UCSC Ensembl
Outerchr2:88876491..88973273hg18UCSC Ensembl
Outerchr2:88934638..89031420hg17UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3896784
hg1996783
hg1896783
hg1796783
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7318
Supporting Variants
SamplesNA18555
Known GenesANKRD36BP2, MIR4436A
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv2272
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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