A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952801



Internal ID16954988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:9748205..9759104hg38UCSC Ensembl
Outerchr12:9900801..9911700hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3810900
hg1910900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999680
SamplesBILGI_BIOE
Known GenesCD69
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952801
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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