A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7360



Internal ID15552362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:49240233..49325502hg38UCSC Ensembl
Outerchr4:49242250..49327519hg19UCSC Ensembl
Outerchr4:48937007..49022276hg18UCSC Ensembl
Outerchr4:49083178..49168447hg17UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3885270
hg1985270
hg1885270
hg1785270
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10405, nssv385, nssv11083, nssv2464, nssv7082, nssv9640, nssv9392, nssv4741
SamplesNA18507, NA12156, NA18956, NA15510, NA18555, NA18517, NA19240, NA19129
Known Genes
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)nsv7360
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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