A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv619355



Internal ID15471250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:197623882..197737338hg38UCSC Ensembl
Outerchr3:197350753..197464209hg19UCSC Ensembl
Outerchr3:198835150..198948606hg18UCSC Ensembl
Outerchr3:198839063..198952519hg17UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg384085
hg194085
hg184085
hg174085
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv508983
Supporting Variants
SamplesNA10860
Known GenesKIAA0226, LOC220729, MIR922
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)nssv619355
Frequency
Sample Size4
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer