A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000007



Internal ID17292959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:59918246..59932945hg38UCSC Ensembl
Outerchr20:58493301..58508000hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3814700
hg1914700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv955145
Supporting Variants
SamplesBILGI_BIOE
Known GenesSYCP2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000007
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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