A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3310



Internal ID15191352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:186167425..186182155hg38UCSC Ensembl
Outerchr4:187088579..187103309hg19UCSC Ensembl
Outerchr4:187325573..187340303hg18UCSC Ensembl
Outerchr4:187463728..187478458hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3814731
hg1914731
hg1814731
hg1714731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4642
Supporting Variants
SamplesNA12878
Known GenesFAM149A
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)nssv3310
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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