A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6300



Internal ID15190878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:134102353..134120157hg38UCSC Ensembl
Outerchr9:136967475..136985279hg19UCSC Ensembl
Outerchr9:135957296..135975100hg18UCSC Ensembl
Outerchr9:133997029..134014833hg17UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3817805
hg1917805
hg1817805
hg1717805
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6751
Supporting Variants
SamplesNA12156
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)nssv6300
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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