A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8318



Internal ID15535546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:156118571..156152024hg38UCSC Ensembl
Outerchr6:156439705..156473158hg19UCSC Ensembl
Outerchr6:156481397..156514850hg18UCSC Ensembl
Outerchr6:156531818..156565271hg17UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg385984
hg195984
hg185984
hg175984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555
Supporting Variants
SamplesNA12156
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)nssv8318
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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