A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5576



Internal ID15550399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:2111661..2146227hg38UCSC Ensembl
Outerchr10:2153855..2188421hg19UCSC Ensembl
Outerchr10:2143855..2178421hg18UCSC Ensembl
Outerchr10:2143855..2178421hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg385423
hg195423
hg185423
hg175423
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2819
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)nsv5576
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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