A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1789



Internal ID15194386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:81693571..81738337hg38UCSC Ensembl
Outerchr9:84308486..84353252hg19UCSC Ensembl
Outerchr9:83498306..83543072hg18UCSC Ensembl
Outerchr9:81538040..81582806hg17UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3844767
hg1944767
hg1844767
hg1744767
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582
Supporting Variants
SamplesNA18555
Known GenesLOC101927502
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)nssv1789
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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