A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4544



Internal ID15549264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:149058648..149105171hg38UCSC Ensembl
Outerchr4:149979800..150026323hg19UCSC Ensembl
Outerchr4:150199250..150245773hg18UCSC Ensembl
Outerchr4:150337405..150383928hg17UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3846524
hg1946524
hg1846524
hg1746524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10424
SamplesNA18956
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)nsv4544
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