A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6749



Internal ID15551689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:133298052..133330043hg38UCSC Ensembl
Outerchr9:136173627..136196879hg19UCSC Ensembl
Outerchr9:135163448..135186700hg18UCSC Ensembl
Outerchr9:133203181..133226433hg17UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg389135
hg199135
hg189135
hg179135
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6299, nssv9475, nssv1808, nssv9926, nssv10690, nssv841, nssv11206, nssv5189, nssv3755
SamplesNA18507, NA12156, NA12878, NA18956, NA15510, NA18555, NA18517, NA19240, NA19129
Known Genes
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)nsv6749
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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