A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8619



Internal ID15535245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:82951744..82996574hg38UCSC Ensembl
Outerchr9:85566659..85611489hg19UCSC Ensembl
Outerchr9:84756479..84801309hg18UCSC Ensembl
Outerchr9:82796213..82841043hg17UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3844831
hg1944831
hg1844831
hg1744831
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585
Supporting Variants
SamplesNA12156
Known GenesRASEF
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)nssv8619
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