A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10356



Internal ID15542442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:112157577..112167424hg38UCSC Ensembl
Outerchr3:111876424..111886271hg19UCSC Ensembl
Outerchr3:113359114..113368961hg18UCSC Ensembl
Outerchr3:113359114..113368961hg17UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg388233
hg198233
hg188233
hg178233
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3948
Supporting Variants
SamplesNA18956
Known GenesSLC9C1
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)nssv10356
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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