A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624320



Internal ID15822893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:155902204..155966824hg38UCSC Ensembl
Outerchr7:155694898..155759518hg19UCSC Ensembl
Outerchr7:155387659..155452279hg18UCSC Ensembl
Outerchr7:155194374..155258994hg17UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3864621
hg1964621
hg1864621
hg1764621
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv510971
Supporting Variants
SamplesNA18994
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)nssv624320
Frequency
Sample Size4
Observed Gain0
Observed Loss0
Observed Complex1
Frequencyn/a


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