A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10282



Internal ID15195830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:9616835..9626939hg38UCSC Ensembl
Outerchr1:9676893..9686997hg19UCSC Ensembl
Outerchr1:9599480..9609584hg18UCSC Ensembl
Outerchr1:9611159..9621263hg17UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg387247
hg197247
hg187247
hg177247
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2187
Supporting Variants
SamplesNA18956
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)nssv10282
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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