A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5796



Internal ID15203955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:76294172..76304514hg38UCSC Ensembl
Outerchr7:75923489..75933831hg19UCSC Ensembl
Outerchr7:75761425..75771767hg18UCSC Ensembl
Outerchr7:75568140..75578482hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg386480
hg196480
hg186480
hg176480
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10560
SamplesNA18956
Known GenesHSPB1
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)nsv5796
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