A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5444



Internal ID15203568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:111658463..111690809hg38UCSC Ensembl
Outerchr6:111979666..112012012hg19UCSC Ensembl
Outerchr6:112086359..112118705hg18UCSC Ensembl
Outerchr6:112086359..112118705hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg387161
hg197161
hg187161
hg177161
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10515
SamplesNA18956
Known GenesFYN
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)nsv5444
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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