A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1788



Internal ID15546351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:87141066..87157721hg38UCSC Ensembl
Outerchr1:87606749..87623404hg19UCSC Ensembl
Outerchr1:87379337..87395992hg18UCSC Ensembl
Outerchr1:87318770..87335425hg17UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg388436
hg198436
hg188436
hg178436
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10101
SamplesNA18956
Known GenesLINC01140
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)nsv1788
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