A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3746



Internal ID15548386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:28432472..28464897hg38UCSC Ensembl
Outerchr3:28473963..28506388hg19UCSC Ensembl
Outerchr3:28448967..28481392hg18UCSC Ensembl
Outerchr3:28448967..28481392hg17UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg387322
hg197322
hg187322
hg177322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3153
SamplesNA12878
Known GenesZCWPW2
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)nsv3746
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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