A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954813



Internal ID16957000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:13700006..13727105hg38UCSC Ensembl
Outerchr1:14026501..14053600hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3827100
hg1927100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003086
SamplesBILGI_BIOE
Known GenesPRDM2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954813
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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