A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4544



Internal ID15539271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:55853680..55868955hg38UCSC Ensembl
Outerchr20:54428736..54444011hg19UCSC Ensembl
Outerchr20:53862143..53877418hg18UCSC Ensembl
Outerchr20:53862143..53877418hg17UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3815276
hg1915276
hg1815276
hg1715276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3420
Supporting Variants
SamplesNA12878
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)nssv4544
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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