A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9770



Internal ID15540096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:115782301..115799426hg38UCSC Ensembl
Outerchr9:118544580..118561705hg19UCSC Ensembl
Outerchr9:117584401..117601526hg18UCSC Ensembl
Outerchr9:115624134..115641259hg17UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3819562
hg1919562
hg1819562
hg1719562
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6683
Supporting Variants
SamplesNA18507
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)nssv9770
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