A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4139



Internal ID15538866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:20395225..22296022hg38UCSC Ensembl
Outerchr15:20600478..22583973hg19UCSC Ensembl
Outerchr15:18860492..20085337hg18UCSC Ensembl
Outerchr15:18860492..20085337hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381900798
hg191983496
hg181224846
hg171224846
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7260
Supporting Variants
SamplesNA12878
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
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)nssv4139
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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