A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997873



Internal ID16944139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:170282197..170298396hg38UCSC Ensembl
Outerchr5:169709201..169725400hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3816200
hg1916200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950440
Supporting Variants
SamplesBILGI_BIOE
Known GenesLCP2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997873
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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