A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10803



Internal ID15541995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:32183870..32192069hg38UCSC Ensembl
Outerchr1:32649471..32657670hg19UCSC Ensembl
Outerchr1:32422058..32430257hg18UCSC Ensembl
Outerchr1:32318564..32326763hg17UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg386761
hg196761
hg186761
hg176761
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7745
Supporting Variants
SamplesNA18956
Known GenesTXLNA
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)nssv10803
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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