A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3752



Internal ID15538480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:125809485..125815255hg38UCSC Ensembl
Outerchr9:128571764..128577534hg19UCSC Ensembl
Outerchr9:127611585..127617355hg18UCSC Ensembl
Outerchr9:125651318..125657088hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg385607
hg195607
hg185607
hg175607
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6715
Supporting Variants
SamplesNA12878
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)nssv3752
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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