A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2926



Internal ID15541628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:93967081..94001449hg38UCSC Ensembl
Outerchr14:94433427..94467795hg19UCSC Ensembl
Outerchr14:93503180..93537548hg18UCSC Ensembl
Outerchr14:93503180..93537548hg17UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg385658
hg195658
hg185658
hg175658
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1405
Supporting Variants
SamplesNA18555
Known GenesASB2, LINC00521
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)nssv2926
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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