A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6109



Internal ID15537754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:170387559..170399071hg38UCSC Ensembl
Outerchr6:170696647..170708159hg19UCSC Ensembl
Outerchr6:170538572..170550084hg18UCSC Ensembl
Outerchr6:170614279..170625791hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3810381
hg1910381
hg1810381
hg1710381
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605
Supporting Variants
SamplesNA12156
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)nssv6109
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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