A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3491



Internal ID15538219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:169547410..169569591hg38UCSC Ensembl
Outerchr6:169947506..169969687hg19UCSC Ensembl
Outerchr6:169689431..169711612hg18UCSC Ensembl
Outerchr6:169765138..169787319hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg385871
hg195871
hg185871
hg175871
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5600
Supporting Variants
SamplesNA12878
Known GenesWDR27
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)nssv3491
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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