A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7942



Internal ID15535922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:30816463..30849861hg38UCSC Ensembl
Outerchr4:30818085..30851483hg19UCSC Ensembl
Outerchr4:30427183..30460581hg18UCSC Ensembl
Outerchr4:30494354..30527752hg17UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg386038
hg196038
hg186038
hg176038
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4286
Supporting Variants
SamplesNA12156
Known GenesPCDH7
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)nssv7942
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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