A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4432



Internal ID15192473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:88795597..88884519hg38UCSC Ensembl
Outerchr2:89095114..89184035hg19UCSC Ensembl
Outerchr2:88876229..88965150hg18UCSC Ensembl
Outerchr2:88934376..89023297hg17UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3888923
hg1988922
hg1888922
hg1788922
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)nssv4432
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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