A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4195



Internal ID15192236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:14654306..14732489hg38UCSC Ensembl
Outerchr16:14748163..14826346hg19UCSC Ensembl
Outerchr16:14655664..14733847hg18UCSC Ensembl
Outerchr16:14655664..14733847hg17UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3878184
hg1978184
hg1878184
hg1778184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1740
Supporting Variants
SamplesNA12878
Known GenesBFAR, NPIPA2, NPIPA3, PLA2G10
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)nssv4195
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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