A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10925



Internal ID15539513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:20419333..22273761hg38UCSC Ensembl
Outerchr15:20624586..22561712hg19UCSC Ensembl
Outerchr15:18884600..20063076hg18UCSC Ensembl
Outerchr15:18884600..20063076hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381854429
hg191937127
hg181178477
hg171178477
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7260
Supporting Variants
SamplesNA15510
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)nssv10925
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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