A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5184



Internal ID15549968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:6163785..6196731hg38UCSC Ensembl
Outerchr6:6164018..6196964hg19UCSC Ensembl
Outerchr6:6109017..6141963hg18UCSC Ensembl
Outerchr6:6109017..6141963hg17UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg388057
hg198057
hg188057
hg178057
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv524
SamplesNA19240
Known GenesF13A1
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)nsv5184
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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