A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4370



Internal ID15549073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:67244933..67273181hg38UCSC Ensembl
Outerchr4:68110651..68138899hg19UCSC Ensembl
Outerchr4:67793246..67821494hg18UCSC Ensembl
Outerchr4:67939417..67967665hg17UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3811484
hg1911484
hg1811484
hg1711484
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3260
SamplesNA12878
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)nsv4370
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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