A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10960



Internal ID15539548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:106831678..106862509hg38UCSC Ensembl
Outerchr1:107374300..107405131hg19UCSC Ensembl
Outerchr1:107175823..107206654hg18UCSC Ensembl
Outerchr1:107086342..107117173hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg389044
hg199044
hg189044
hg179044
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2254
Supporting Variants
SamplesNA15510
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)nssv10960
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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