A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4691



Internal ID15543054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:151664137..151670720hg38UCSC Ensembl
Outerchr3:151381925..151388508hg19UCSC Ensembl
Outerchr3:152864615..152871198hg18UCSC Ensembl
Outerchr3:152864623..152871206hg17UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3810270
hg1910270
hg1810270
hg1710270
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4066
Supporting Variants
SamplesNA19129
Known GenesMIR548H2
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)nssv4691
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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