A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3897



Internal ID15538624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:106688506..106722759hg38UCSC Ensembl
Outerchr10:108448264..108482517hg19UCSC Ensembl
Outerchr10:108438254..108472507hg18UCSC Ensembl
Outerchr10:108438254..108472507hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg385480
hg195480
hg185480
hg175480
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7540
Supporting Variants
SamplesNA12878
Known GenesSORCS1
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)nssv3897
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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