A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4431



Internal ID15192472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:88795794..90209331hg38UCSC Ensembl
Outerchr2:89095311..90248197hg19UCSC Ensembl
Outerchr2:88876426..89885502hg18UCSC Ensembl
Outerchr2:88934573..89943649hg17UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg381413538
hg191152887
hg181009077
hg171009077
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7318
Supporting Variants
SamplesNA12878
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)nssv4431
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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