A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3003153



Internal ID16949419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:22053808..22107507hg38UCSC Ensembl
Outerchr1:22380301..22434000hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3853700
hg1953700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv954904
Supporting Variants
SamplesBILGI_BIOE
Known GenesCDC42
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3003153
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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