A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6772



Internal ID15551715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:137495408..137535206hg38UCSC Ensembl
Outerchr9:140389860..140429658hg19UCSC Ensembl
Outerchr9:139509681..139549479hg18UCSC Ensembl
Outerchr9:137665697..137705495hg17UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg385335
hg195335
hg185335
hg175335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3760, nssv5194
SamplesNA12878, NA19129
Known GenesPNPLA7
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)nsv6772
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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