A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5660



Internal ID15543771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:2320366..2327841hg38UCSC Ensembl
Outerchr1:2251805..2259280hg19UCSC Ensembl
Outerchr1:2241665..2249140hg18UCSC Ensembl
Outerchr1:2283967..2291442hg17UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg386493
hg196493
hg186493
hg176493
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742
Supporting Variants
SamplesNA19129
Known GenesMORN1
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)nssv5660
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