A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7302



Internal ID15552298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:6926148..6977389hg38UCSC Ensembl
Outerchr18:6926147..6977388hg19UCSC Ensembl
Outerchr18:6916147..6967388hg18UCSC Ensembl
Outerchr18:6916147..6967388hg17UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3851242
hg1951242
hg1851242
hg1751242
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2187
SamplesNA18555
Known GenesLAMA1, LINC00668
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)nsv7302
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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