A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7882



Internal ID15189296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:151408925..151431596hg38UCSC Ensembl
Outerchr3:151126713..151149384hg19UCSC Ensembl
Outerchr3:152609403..152632074hg18UCSC Ensembl
Outerchr3:152609411..152632082hg17UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg385621
hg195621
hg185621
hg175621
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4063
Supporting Variants
SamplesNA12156
Known GenesMED12L
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)nssv7882
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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