A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3101



Internal ID15540874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:81941207..81952631hg38UCSC Ensembl
Outerchr3:81990358..82001782hg19UCSC Ensembl
Outerchr3:82073048..82084472hg18UCSC Ensembl
Outerchr3:82073048..82084472hg17UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg386164
hg196164
hg186164
hg176164
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3893
Supporting Variants
SamplesNA18555
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)nssv3101
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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