A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3735



Internal ID15538463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:104206263..104228924hg38UCSC Ensembl
Outerchr9:106968544..106991205hg19UCSC Ensembl
Outerchr9:106008365..106031026hg18UCSC Ensembl
Outerchr9:104048099..104070760hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg385896
hg195896
hg185896
hg175896
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6649
Supporting Variants
SamplesNA12878
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)nssv3735
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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