A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6671



Internal ID15204918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:112632751..112677737hg38UCSC Ensembl
Outerchr9:115395031..115440017hg19UCSC Ensembl
Outerchr9:114434852..114479838hg18UCSC Ensembl
Outerchr9:112474586..112519572hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3844987
hg1944987
hg1844987
hg1744987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8653
SamplesNA12156
Known GenesKIAA1958
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)nsv6671
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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