A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv619149



Internal ID15817730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:68879882..68885882hg38UCSC Ensembl
Outerchr15:69172221..69178221hg19UCSC Ensembl
Outerchr15:66959275..66965275hg18UCSC Ensembl
Outerchr15:66959275..66965275hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg386001
hg196001
hg186001
hg176001
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv507786
Supporting Variants
SamplesNA10860
Known GenesMIR548H4
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)nssv619149
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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