A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3269



Internal ID15191311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:87928829..87974895hg38UCSC Ensembl
Outerchr4:88849981..88896047hg19UCSC Ensembl
Outerchr4:89069005..89115071hg18UCSC Ensembl
Outerchr4:89207160..89253226hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3846067
hg1946067
hg1846067
hg1746067
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7364
Supporting Variants
SamplesNA12878
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)nssv3269
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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