A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6734



Internal ID15204987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:130491286..130514297hg38UCSC Ensembl
Outerchr9:133366673..133389684hg19UCSC Ensembl
Outerchr9:132356494..132379505hg18UCSC Ensembl
Outerchr9:130396227..130419238hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3823012
hg1923012
hg1823012
hg1723012
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1803
SamplesNA18555
Known GenesASS1
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)nsv6734
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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