A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7489



Internal ID15552503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:91740069..91773470hg38UCSC Ensembl
Outerchr10:93499826..93533227hg19UCSC Ensembl
Outerchr10:93489806..93523207hg18UCSC Ensembl
Outerchr10:93489806..93523207hg17UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg385880
hg195880
hg185880
hg175880
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5305
SamplesNA19129
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)nsv7489
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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