A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2847



Internal ID15541715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:81422662..81457377hg38UCSC Ensembl
Outerchr10:83182418..83217133hg19UCSC Ensembl
Outerchr10:83172398..83207113hg18UCSC Ensembl
Outerchr10:83172398..83207113hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg385310
hg195310
hg185310
hg175310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7387
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)nssv2847
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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