A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603



Internal ID15551529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:88190840..88218783hg38UCSC Ensembl
Outerchr9:90805755..90833698hg19UCSC Ensembl
Outerchr9:89995575..90023518hg18UCSC Ensembl
Outerchr9:88035309..88063252hg17UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3814073
hg1914073
hg1814073
hg1714073
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9472, nssv1791, nssv5167
SamplesNA18555, NA18517, NA19129
Known Genes
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)nsv6603
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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