A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv617733



Internal ID15470202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:37291321..37297321hg38UCSC Ensembl
Outerchr7:37330925..37336925hg19UCSC Ensembl
Outerchr7:37297450..37303450hg18UCSC Ensembl
Outerchr7:37104165..37110165hg17UCSC Ensembl
Cytoband7p14.1
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 Variantsnsv507385
Supporting Variants
SamplesCHM
Known GenesELMO1
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)nssv617733
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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