A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954812



Internal ID16956999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:127039525..127106424hg38UCSC Ensembl
Outerchr2:127797101..127864000hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3866900
hg1966900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001890
SamplesBILGI_BIOE
Known GenesBIN1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954812
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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