A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8559



Internal ID15535305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:132080059..132113488hg38UCSC Ensembl
Outerchr8:133092306..133125735hg19UCSC Ensembl
Outerchr8:133161488..133194917hg18UCSC Ensembl
Outerchr8:133161488..133194917hg17UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg386006
hg196006
hg186006
hg176006
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6401
Supporting Variants
SamplesNA12156
Known GenesHHLA1
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)nssv8559
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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