A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4332



Internal ID15549031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:209539469..209573142hg38UCSC Ensembl
Outerchr1:209712814..209746487hg19UCSC Ensembl
Outerchr1:207779437..207813110hg18UCSC Ensembl
Outerchr1:206101209..206134882hg17UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg386342
hg196342
hg186342
hg176342
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2763
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)nsv4332
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