A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8667



Internal ID15535197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:124522641..124546161hg38UCSC Ensembl
Outerchr9:127284920..127308440hg19UCSC Ensembl
Outerchr9:126324741..126348261hg18UCSC Ensembl
Outerchr9:124364474..124387994hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3823521
hg1923521
hg1823521
hg1723521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6712
Supporting Variants
SamplesNA12156
Known GenesNR6A1
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)nssv8667
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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