A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3201



Internal ID15537929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:138226866..138261906hg38UCSC Ensembl
Outerchr3:137945708..137980748hg19UCSC Ensembl
Outerchr3:139428398..139463438hg18UCSC Ensembl
Outerchr3:139428406..139463446hg17UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg384708
hg194708
hg184708
hg174708
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4030
Supporting Variants
SamplesNA12878
Known GenesARMC8, NME9
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)nssv3201
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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