A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446



Internal ID15549156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:103035403..103058970hg38UCSC Ensembl
Outerchr4:103956560..103980127hg19UCSC Ensembl
Outerchr4:104176009..104199576hg18UCSC Ensembl
Outerchr4:104314164..104337731hg17UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg386156
hg196156
hg186156
hg176156
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3135
SamplesNA18555
Known GenesSLC9B2
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)nsv4446
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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