A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6658



Internal ID15537205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:72287770..72300490hg38UCSC Ensembl
Outerchr1:72753453..72766173hg19UCSC Ensembl
Outerchr1:72526041..72538761hg18UCSC Ensembl
Outerchr1:72465474..72478194hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3812721
hg1912721
hg1812721
hg1712721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1376
Supporting Variants
SamplesNA12156
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv6658
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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