A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7367



Internal ID15552369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:187918185..187997831hg38UCSC Ensembl
Outerchr4:188839339..188918985hg19UCSC Ensembl
Outerchr4:189076333..189155979hg18UCSC Ensembl
Outerchr4:189214488..189294134hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3879647
hg1979647
hg1879647
hg1779647
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7136, nssv9655, nssv9654
SamplesNA18507, NA12156
Known GenesZFP42
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)nsv7367
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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