A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv617523



Internal ID15816678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:76386679..76398451hg38UCSC Ensembl
Outerchr6:77096396..77108168hg19UCSC Ensembl
Outerchr6:77153116..77164888hg18UCSC Ensembl
Outerchr6:77153116..77164888hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3811773
hg1911773
hg1811773
hg1711773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv508413
Supporting Variants
SamplesCHM
Known Genes
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)nssv617523
Frequency
Sample Size4
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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