A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9702



Internal ID15193415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:165280959..165321712hg38UCSC Ensembl
Outerchr6:165694448..165735201hg19UCSC Ensembl
Outerchr6:165614438..165655191hg18UCSC Ensembl
Outerchr6:165664859..165705612hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3840754
hg1940754
hg1840754
hg1740754
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5586
Supporting Variants
SamplesNA18507
Known GenesC6orf118
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)nssv9702
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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