A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4924



Internal ID15549682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:97055747..97101529hg38UCSC Ensembl
Outerchr5:96391451..96437233hg19UCSC Ensembl
Outerchr5:96417207..96462989hg18UCSC Ensembl
Outerchr5:96417207..96462989hg17UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3845783
hg1945783
hg1845783
hg1745783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6013
SamplesNA12156
Known GenesLIX1
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)nsv4924
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer