A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10350



Internal ID15542448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:70891084..70923607hg38UCSC Ensembl
Outerchr3:70940235..70972758hg19UCSC Ensembl
Outerchr3:71022925..71055448hg18UCSC Ensembl
Outerchr3:71022925..71055448hg17UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg386961
hg196961
hg186961
hg176961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3870
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)nssv10350
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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