A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997865



Internal ID16944131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:157268591..157284790hg38UCSC Ensembl
Outerchr5:156695601..156711800hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3816200
hg1916200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950432
Supporting Variants
SamplesBILGI_BIOE
Known GenesCYFIP2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997865
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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