A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv618862



Internal ID15818666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:107744055..107783086hg38UCSC Ensembl
Outerchr9:110506336..110545367hg19UCSC Ensembl
Outerchr9:109546157..109585188hg18UCSC Ensembl
Outerchr9:107585891..107624922hg17UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3839032
hg1939032
hg1839032
hg1739032
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv508561
Supporting Variants
SamplesNA10860
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)nssv618862
Frequency
Sample Size4
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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