A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3872



Internal ID15201839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:71558851..71592872hg38UCSC Ensembl
Outerchr3:71608002..71642023hg19UCSC Ensembl
Outerchr3:71690692..71724713hg18UCSC Ensembl
Outerchr3:71690692..71724713hg17UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg385720
hg195720
hg185720
hg175720
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3174
SamplesNA12878
Known GenesFOXP1
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)nsv3872
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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