A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3723



Internal ID15191765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69116863..69130466hg38UCSC Ensembl
Outerchr9:71731779..71745382hg19UCSC Ensembl
Outerchr9:70921599..70935202hg18UCSC Ensembl
Outerchr9:68961333..68974936hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3813604
hg1913604
hg1813604
hg1713604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550
Supporting Variants
SamplesNA12878
Known GenesTJP2
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)nssv3723
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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