A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3001867



Internal ID17294819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:13109029..13120527hg38UCSC Ensembl
Outerchr1:13176501..13188000hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3811499
hg1911500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953504
Supporting Variants
SamplesBILGI_BIOE
Known GenesHNRNPCP5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3001867
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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