A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2736



Internal ID15541837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:141653181..141687362hg38UCSC Ensembl
Outerchr6:141974318..142008499hg19UCSC Ensembl
Outerchr6:142016011..142050192hg18UCSC Ensembl
Outerchr6:142016011..142050192hg17UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg385850
hg195850
hg185850
hg175850
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5506
Supporting Variants
SamplesNA18555
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)nssv2736
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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