A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3271



Internal ID15537999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:90665589..90689030hg38UCSC Ensembl
Outerchr4:91586740..91610181hg19UCSC Ensembl
Outerchr4:91805763..91829204hg18UCSC Ensembl
Outerchr4:91943918..91967359hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3823442
hg1923442
hg1823442
hg1723442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4419
Supporting Variants
SamplesNA12878
Known GenesCCSER1
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)nssv3271
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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