A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9906



Internal ID15193301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:9613765..9633692hg38UCSC Ensembl
Outerchr1:9673823..9693750hg19UCSC Ensembl
Outerchr1:9596410..9616337hg18UCSC Ensembl
Outerchr1:9608089..9628016hg17UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg387452
hg197452
hg187452
hg177452
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2187
Supporting Variants
SamplesNA18507
Known GenesTMEM201
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)nssv9906
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer