A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2846



Internal ID15195030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:71978618..72012071hg38UCSC Ensembl
Outerchr10:73738376..73771829hg19UCSC Ensembl
Outerchr10:73408382..73441835hg18UCSC Ensembl
Outerchr10:73408382..73441835hg17UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg386567
hg196567
hg186567
hg176567
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7110
Supporting Variants
SamplesNA18555
Known GenesCHST3
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)nssv2846
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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