A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10392



Internal ID15195720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:8620344..8621691hg38UCSC Ensembl
Outerchr4:8622070..8623417hg19UCSC Ensembl
Outerchr4:8672970..8674317hg18UCSC Ensembl
Outerchr4:8740141..8741488hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3813094
hg1913094
hg1813094
hg1713094
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4225
Supporting Variants
SamplesNA18956
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)nssv10392
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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