A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4646



Internal ID15549376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:186536664..186571366hg38UCSC Ensembl
Outerchr4:187457818..187492520hg19UCSC Ensembl
Outerchr4:187694812..187729514hg18UCSC Ensembl
Outerchr4:187832967..187867669hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg386295
hg196295
hg186295
hg176295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv437
SamplesNA19240
Known GenesMTNR1A
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)nsv4646
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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