A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv619352



Internal ID15471247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:196810982..196810982hg38UCSC Ensembl
Outerchr3:196537853..196537853hg19UCSC Ensembl
Outerchr3:198022250..198022250hg18UCSC Ensembl
Outerchr3:198026163..198026163hg17UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg389734
hg199734
hg189734
hg179734
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv508979
Supporting Variants
SamplesNA10860
Known GenesPAK2
MethodOptical mapping
AnalysisSingle-molecule optical maps were assembled into genome-wide consensus maps. These consensus maps were compared to a restriction map generated from the NCBI b35 human genome reference sequence.
PlatformOptical Mapping
Comments
ReferenceTeague_et_al_2010
Pubmed ID20534489
Accession Number(s)nssv619352
Frequency
Sample Size4
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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