A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9880



Internal ID15539957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:186417747..186445186hg38UCSC Ensembl
Outerchr4:187338901..187366340hg19UCSC Ensembl
Outerchr4:187575895..187603334hg18UCSC Ensembl
Outerchr4:187714050..187741489hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg388207
hg198207
hg188207
hg178207
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4645
Supporting Variants
SamplesNA18507
Known GenesF11-AS1
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)nssv9880
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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