A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953801



Internal ID16955988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:30245980..30290479hg38UCSC Ensembl
Outerchr16:30257301..30301800hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3844500
hg1944500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000073
SamplesBILGI_BIOE
Known GenesLOC440354, LOC595101
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953801
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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