A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv620398



Internal ID15819753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:154752340..154758340hg38UCSC Ensembl
Outerchr7:154544050..154550050hg19UCSC Ensembl
Outerchr7:154174983..154180983hg18UCSC Ensembl
Outerchr7:153981698..153987698hg17UCSC Ensembl
Cytoband7q36.2
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 Variantsnsv507428
Supporting Variants
SamplesNA15510
Known GenesDPP6
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)nssv620398
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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