A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10116



Internal ID15195995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:93095373..93127336hg38UCSC Ensembl
Outerchr1:93560930..93592893hg19UCSC Ensembl
Outerchr1:93333518..93365481hg18UCSC Ensembl
Outerchr1:93272951..93304914hg17UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg387510
hg197510
hg187510
hg177510
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1866
Supporting Variants
SamplesNA18956
Known GenesMTF2
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)nssv10116
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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