A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9653



Internal ID15540150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:181240750..181243637hg38UCSC Ensembl
Outerchr4:182161903..182164790hg19UCSC Ensembl
Outerchr4:182398897..182401784hg18UCSC Ensembl
Outerchr4:182537052..182539939hg17UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3818869
hg1918869
hg1818869
hg1718869
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4621
Supporting Variants
SamplesNA18507
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)nssv9653
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