A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6728



Internal ID15551666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:129752333..129784235hg38UCSC Ensembl
Outerchr9:132514612..132546514hg19UCSC Ensembl
Outerchr9:131554433..131586335hg18UCSC Ensembl
Outerchr9:129594166..129626068hg17UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3831903
hg1931903
hg1831903
hg1731903
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5183
SamplesNA19129
Known GenesPTGES
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)nsv6728
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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