A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9036



Internal ID15534828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:62596801..62608554hg38UCSC Ensembl
Outerchr12:62990581..63002334hg19UCSC Ensembl
Outerchr12:61276848..61288601hg18UCSC Ensembl
Outerchr12:61276848..61288601hg17UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg386462
hg196462
hg186462
hg176462
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv740
Supporting Variants
SamplesNA12156
Known GenesC12orf61, MIRLET7I, MON2
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)nssv9036
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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