A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8238



Internal ID15535626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:39552384..39586110hg38UCSC Ensembl
Outerchr6:39520160..39553886hg19UCSC Ensembl
Outerchr6:39628138..39661864hg18UCSC Ensembl
Outerchr6:39628138..39661864hg17UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg385714
hg195714
hg185714
hg175714
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5271
Supporting Variants
SamplesNA12156
Known GenesKIF6
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)nssv8238
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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