A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1889



Internal ID15541172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:34073344..34106580hg38UCSC Ensembl
Outerchr10:34362272..34395508hg19UCSC Ensembl
Outerchr10:34402278..34435514hg18UCSC Ensembl
Outerchr10:34402278..34435514hg17UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg386786
hg196786
hg186786
hg176786
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6310
Supporting Variants
SamplesNA18555
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)nssv1889
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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