A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1039



Internal ID15198403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:31416955..31440344hg38UCSC Ensembl
Outerchr1:31889802..31913191hg19UCSC Ensembl
Outerchr1:31662389..31685778hg18UCSC Ensembl
Outerchr1:31558895..31582284hg17UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg386882
hg196882
hg186882
hg176882
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7712
Supporting Variants
SamplesNA19240
Known GenesSERINC2
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)nssv1039
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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