A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv618660



Internal ID15816466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:158539228..158629651hg38UCSC Ensembl
Outerchr7:158331920..158422343hg19UCSC Ensembl
Outerchr7:158024681..158115104hg18UCSC Ensembl
Outerchr7:157831396..157921819hg17UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3890424
hg1990424
hg1890424
hg1790424
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv510974
Supporting Variants
SamplesCHM
Known GenesMIR5707, PTPRN2
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)nssv618660
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex1
Frequencyn/a


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