A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5174



Internal ID15196150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:105680551..105714206hg38UCSC Ensembl
Outerchr9:108442832..108476487hg19UCSC Ensembl
Outerchr9:107482653..107516308hg18UCSC Ensembl
Outerchr9:105522387..105556042hg17UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg385621
hg195621
hg185621
hg175621
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6653
Supporting Variants
SamplesNA19129
Known GenesTMEM38B
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)nssv5174
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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