A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9648



Internal ID15540155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:148815719..148832222hg38UCSC Ensembl
Outerchr4:149736871..149753374hg19UCSC Ensembl
Outerchr4:149956321..149972824hg18UCSC Ensembl
Outerchr4:150094476..150110979hg17UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3820192
hg1920192
hg1820192
hg1720192
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4542
Supporting Variants
SamplesNA18507
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)nssv9648
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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