A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2497



Internal ID15193942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:186164028..186193447hg38UCSC Ensembl
Outerchr4:187085182..187114601hg19UCSC Ensembl
Outerchr4:187322176..187351595hg18UCSC Ensembl
Outerchr4:187460331..187489750hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3829420
hg1929420
hg1829420
hg1729420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4642
Supporting Variants
SamplesNA18555
Known GenesCYP4V2, FAM149A, FLJ38576
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)nssv2497
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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