A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3870



Internal ID15548523
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 StatusM
Merged Variants
Supporting Variantsnssv10350
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)nsv3870
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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