A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3733



Internal ID15538461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:100521235..100550169hg38UCSC Ensembl
Outerchr9:103283517..103312451hg19UCSC Ensembl
Outerchr9:102323338..102352272hg18UCSC Ensembl
Outerchr9:100363072..100392006hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3810786
hg1910786
hg1810786
hg1710786
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6639
Supporting Variants
SamplesNA12878
Known GenesMSANTD3-TMEFF1, TMEFF1
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)nssv3733
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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