A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9899



Internal ID15539979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:170398824..170417406hg38UCSC Ensembl
Outerchr6:170707912..170726494hg19UCSC Ensembl
Outerchr6:170549837..170568419hg18UCSC Ensembl
Outerchr6:170625544..170644126hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3810742
hg1910742
hg1810742
hg1710742
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605
Supporting Variants
SamplesNA18507
Known GenesFAM120B
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)nssv9899
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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