A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7790



Internal ID15189388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:39240511..39273967hg38UCSC Ensembl
Outerchr3:39282002..39315458hg19UCSC Ensembl
Outerchr3:39257006..39290462hg18UCSC Ensembl
Outerchr3:39257006..39290462hg17UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg385980
hg195980
hg185980
hg175980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3772
Supporting Variants
SamplesNA12156
Known GenesCX3CR1
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)nssv7790
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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