A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7989



Internal ID15535875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:111705417..111715320hg38UCSC Ensembl
Outerchr4:112626573..112636476hg19UCSC Ensembl
Outerchr4:112846022..112855925hg18UCSC Ensembl
Outerchr4:112984177..112994080hg17UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg386700
hg196700
hg186700
hg176700
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4468
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)nssv7989
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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