A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv619748



Internal ID15471643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:34228715..34287224hg38UCSC Ensembl
Outerchr19:34719620..34778129hg19UCSC Ensembl
Outerchr19:39411460..39469969hg18UCSC Ensembl
Outerchr19:39411460..39469969hg17UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg386075
hg196075
hg186075
hg176075
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv509737
Supporting Variants
SamplesNA10860
Known GenesKIAA0355, LSM14A
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)nssv619748
Frequency
Sample Size4
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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