A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625227



Internal ID15502077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:34653416..34656492hg38UCSC Ensembl
Outerchr20:33241220..33244296hg19UCSC Ensembl
Outerchr20:32704881..32707957hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg383077
hg193077
hg183077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512614
Supporting Variants
Samples1
Known GenesPIGU
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv625227
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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