A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv431



Internal ID15544906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:177449547..177474264hg38UCSC Ensembl
Outerchr4:178370701..178395418hg19UCSC Ensembl
Outerchr4:178607695..178632412hg18UCSC Ensembl
Outerchr4:178745850..178770567hg17UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3824718
hg1924718
hg1824718
hg1724718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4614
Supporting Variants
SamplesNA19240
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)nssv431
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