A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2584



Internal ID15540532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:35788553..35789650hg38UCSC Ensembl
Outerchr6:35756330..35757427hg19UCSC Ensembl
Outerchr6:35864308..35865405hg18UCSC Ensembl
Outerchr6:35864308..35865405hg17UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3810674
hg1910674
hg1810674
hg1710674
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5259
Supporting Variants
SamplesNA18555
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)nssv2584
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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