A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7082



Internal ID15536782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:49261394..49325502hg38UCSC Ensembl
Outerchr4:49263411..49327519hg19UCSC Ensembl
Outerchr4:48958168..49022276hg18UCSC Ensembl
Outerchr4:49104339..49168447hg17UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3864109
hg1964109
hg1864109
hg1764109
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7360
Supporting Variants
SamplesNA12156
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)nssv7082
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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