A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3001752



Internal ID16948018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:72126972..72160571hg38UCSC Ensembl
Outerchr2:72354101..72387700hg19UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg3833600
hg1933600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953147
Supporting Variants
SamplesBILGI_BIOE
Known GenesCYP26B1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3001752
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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