A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7549



Internal ID8519551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:111080506..111096106hg38UCSC Ensembl
Outerchr10:112840264..112855864hg19UCSC Ensembl
Outerchr10:112830254..112845854hg18UCSC Ensembl
Outerchr10:112830254..112845854hg17UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg385870
hg195870
hg185870
hg175870
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5318
SamplesNA19129
Known GenesADRA2A
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)nsv7549
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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