A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7693



Internal ID15536171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:57034206..57078954hg38UCSC Ensembl
Outerchr20:55609262..55654010hg19UCSC Ensembl
Outerchr20:55042669..55087417hg18UCSC Ensembl
Outerchr20:55042669..55087417hg17UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3844749
hg1944749
hg1844749
hg1744749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3423
Supporting Variants
SamplesNA12156
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)nssv7693
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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