A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9476



Internal ID15193504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137714382..137730970hg38UCSC Ensembl
Outerchr9:140608834..140625422hg19UCSC Ensembl
Outerchr9:139728655..139745243hg18UCSC Ensembl
Outerchr9:137884671..137901259hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3815532
hg1915532
hg1815532
hg1715532
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6773
Supporting Variants
SamplesNA18517
Known GenesEHMT1
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)nssv9476
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