A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv622708



Internal ID15474595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:76502002..76521491hg38UCSC Ensembl
Outerchr10:78261760..78281249hg19UCSC Ensembl
Outerchr10:77931766..77951255hg18UCSC Ensembl
Outerchr10:77931766..77951255hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3819490
hg1919490
hg1819490
hg1719490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv508594
Supporting Variants
SamplesNA18994
Known GenesC10orf11
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)nssv622708
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