A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7406



Internal ID15552412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:131750140..131793499hg38UCSC Ensembl
Outerchr7:131434899..131478258hg19UCSC Ensembl
Outerchr7:131085439..131128798hg18UCSC Ensembl
Outerchr7:130892154..130935513hg17UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3843360
hg1943360
hg1843360
hg1743360
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv684
SamplesNA19240
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)nsv7406
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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