A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv622700



Internal ID15474587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:71870979..71930836hg38UCSC Ensembl
Outerchr10:73630737..73690594hg19UCSC Ensembl
Outerchr10:73300743..73360600hg18UCSC Ensembl
Outerchr10:73300743..73360600hg17UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3859858
hg1959858
hg1859858
hg1759858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv508591
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)nssv622700
Frequency
Sample Size4
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer