A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10684



Internal ID15542114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:125812695..125829236hg38UCSC Ensembl
Outerchr9:128574974..128591515hg19UCSC Ensembl
Outerchr9:127614795..127631336hg18UCSC Ensembl
Outerchr9:125654528..125671069hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg387114
hg197114
hg187114
hg177114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6715
Supporting Variants
SamplesNA18956
Known GenesPBX3
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)nssv10684
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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