A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2625



Internal ID15540487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:160781175..160794426hg38UCSC Ensembl
Outerchr6:161202207..161215458hg19UCSC Ensembl
Outerchr6:161122197..161135448hg18UCSC Ensembl
Outerchr6:161172618..161185869hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg388304
hg198304
hg188304
hg178304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5573
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)nssv2625
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